'en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)'
(id=16821349 ; fe=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=11857 creation date=2021-07-24 touchdate=2025-07-25 19:48:18.000)

≈ 1122 relations sortantes en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:21-hydroxylase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:22q telomere deletion syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:22q telomere deletion syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:3-methylglutaconic aciduria type 3 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:5 alpha steroid reductase 2 deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:acid phosphatase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:alpha dystroglycanopathies n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alpha dystroglycanopathies | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:anterior chamber malformation (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:anterior chamber malformation (wws) | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:antiphospholipid syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:antiphospholipid syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:ataxia with vitamin e deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:ateliotic dwarfism without insulinopenia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:ayala's disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ayala's disease | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:becker generalized myotonia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:brachydactyly syndrome type b n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:brody myopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:brody myopathy | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:camurati-engelmann syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:camurati-engelmann syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:cardiofaciocutaneous syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cardiofaciocutaneous syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:chediak-higashi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chediak-higashi syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:choreoathetosis/spasticity, episodic n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:chronic infantile neurological cutaneous and articular syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chronic infantile neurological cutaneous and articular syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:citrin deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:coffin-lowry syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:coffin-lowry syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:congenital dyserythropoietic anemia, type ii n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:congenital malformation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital malformation syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:congenital sucrase-isomaltase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:conn syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:conn syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:crisponi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:cystinosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cystinosis | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:cytochrome-c oxidase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:deafness, sensorineural, and male infertility n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:deletion 18p syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:deletion 18p syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:dentatorubral-pallidoluysian atrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:donohue syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:ectrodactyly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ectrodactyly | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:ehlers-danlos syndrome, arthrochalasia type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:familial atypical hemolytic uremic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial atypical hemolytic uremic syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:familial c3b inhibitor deficiency syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:floating-harbor syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:floating-harbor syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:folinic acid responsive seizure syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:folinic acid responsive seizure syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:frasier syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:frasier syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:geroderma osteodysplastica n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:glucose transporter protein type 1 deficiency syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glucose transporter protein type 1 deficiency syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:hereditary optic atrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary optic atrophy | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:hnsha due to aldolase a deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hnsha due to aldolase a deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:hypospadias-mental retardation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:infantile hypophosphatasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:insulin autoimmune syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:insulin autoimmune syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:jeune syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:jeune syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:kohlschutter tonz syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kohlschutter tonz syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:kshv inflammatory cytokine syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kshv inflammatory cytokine syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:lateral medullary syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lateral medullary syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:lesch-nyhan syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:leukodystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:limb-girdle muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:limb-girdle muscular dystrophy | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:lipoid proteinosis of urbach and wiethe n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:mallory-weiss syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mallory-weiss syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:menopausal muscular dystrophy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:menopausal muscular dystrophy syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:microcephaly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microcephaly | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:muscle amp deaminase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:muscular dystrophy-deafmutism syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy-deafmutism syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:nance-horan syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:non-polyposis turcot syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:non-polyposis turcot syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:oculo-palato-digital syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:oculo-palato-digital syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:oculocerebrorenal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:optic nerve hypoplasia (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:optic nerve hypoplasia (wws) | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:organic brain syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:organic brain syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:orotic aciduria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:overlap syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:overlap syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:pachygyria with preferential frontoparietal involvement (meb) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pachygyria with preferential frontoparietal involvement (meb) | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:patients with meb may acquire ability to walk and a few words n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:patients with meb may acquire ability to walk and a few words | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:peeling skin syndrome, acral type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:perlman syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:perlman syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:pharmacotherapeutic n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pharmacotherapeutic | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:pituitary adenoma, familial isolated (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:poems syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:poems syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:potocki-lupski syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:potocki-lupski syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:primary fanconi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:primary fanconi syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:progressive familial intrahepatic cholestasis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:progressive familial intrahepatic cholestasis | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:progressive supranuclear palsy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:progressive supranuclear palsy | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:pyruvate carboxylase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:radial aplasia-thrombocytopenia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:radial aplasia-thrombocytopenia syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:radiotherapeutic n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:radiotherapeutic | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:roentgenographic n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:roentgenographic | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:sandifer's syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sandifer's syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:sellars beighton syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sellars beighton syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:severe early childhood onset retinal dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:severe steroid 21-hydroxylase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:simpson golabi behmel syndrome type 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:sjogren syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sjogren syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:smith-lemli-opitz syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:smith-lemli-opitz syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:smith-mccort dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:spastic ataxia, charlevoix-saguenay type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:stevens-johnson syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:stevens-johnson syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:stiff person syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:stiff person syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:taxonomic n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:taxonomic | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:transcobalamin ii deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:veterinary aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:veterinary aspects | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:waterhouse-friderichsen syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:waterhouse-friderichsen syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:weaver syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:weaver syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:white matter changes n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:white matter changes | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:wolf-hirschhorn syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> en:xxyy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:xxyy syndrome | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 30 / 1 -> syndrome de Warburg n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=syndrome de Warburg | rel=r_associated | relid=0 | w=30 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> dystroglycanopathies n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=dystroglycanopathies | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:17q21 microdeletion syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:17q21 microdeletion syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:3-methylglutaconic aciduria type 5 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:aagenaes syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aagenaes syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:achard syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:achard syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:aicardi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:albinism n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:albinism | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:alice in wonderland syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alice in wonderland syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:alpha-1 antitrypsin deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:alpha, alpha-trehalase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:aminomethyltransferase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:arginine:glycine amidinotransferase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:ataxia telangiectasia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:autoinflammation, lipodystrophy and dermatosis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autoinflammation, lipodystrophy and dermatosis syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:autosomal recessive ichthyosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive ichthyosis | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:behr syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:behr syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:biotinidase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:cardiorenal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cardiorenal syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:chromosome 16p11.2 deletion syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chromosome 16p11.2 deletion syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:cobblestone lissencephaly, type ii (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cobblestone lissencephaly, type ii (wws) | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:coloboma (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:coloboma (wws) | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:congenital n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:congenital disorder of glycosylation type ig n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:congenital muscular dystrophy with arthrogryposis multiplex congenita n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital muscular dystrophy with arthrogryposis multiplex congenita | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:congenital pancreatic enterokinase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:cryptophthalmos syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:cutis laxa, autosomal recessive n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:de sanctis-cacchione syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:deletion 18q syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:deletion 18q syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:disorganized brain cytoarchitecture n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:disorganized brain cytoarchitecture | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:double cortex syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:double cortex syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:drug hypersensitivity syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:drug hypersensitivity syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:encephalopathy due to sulfite oxidase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:erb's muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:erb's muscular dystrophy | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:escobar syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:escobar syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:fused hemispheres (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fused hemispheres (wws) | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:gardner syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gardner syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:genetic disorder n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:genetic disorder | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:glaucoma n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glaucoma | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:glycogen storage disease type iib n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glycogen storage disease type iib | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:griscelli syndrome type 2 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:griscelli syndrome type 2 | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:gyrate atrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gyrate atrophy | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:hard skin syndrome parana type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hard skin syndrome parana type | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:hemophagocytic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hemophagocytic syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:hepatorenal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hepatorenal syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:hyperplastic primary vitreous (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hyperplastic primary vitreous (wws) | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:hypoplastic left heart syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypoplastic left heart syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:hypoplastic right heart syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypoplastic right heart syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:immunodeficiency syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:immunodeficiency syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:iris malformation or hypoplasia (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:iris malformation or hypoplasia (wws) | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:isolated hypoplasia of the right ventricle n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:kabuki syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:kallmann syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:kaufman-mckusick syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kaufman-mckusick syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:kawasaki disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kawasaki disease | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:kluver-bucy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kluver-bucy syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:laurence-moon syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:lissencephaly, x-linked, 2 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lissencephaly, x-linked, 2 | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:long qt syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:long qt syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:marfan syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:masa syndrome (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:meckel-gruber syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:meckel-gruber syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:merrf syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:merrf syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:microcephaly deafness syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:microcephaly microcornea syndrome seemanova type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:morm syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:morm syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4 | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:nursing therapy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:nursing therapy | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:otopalatodigital syndrome type 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:otopalatodigital syndrome type 1 | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:paraneoplastic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:paraneoplastic syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:penta x syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:penta x syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:poland syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:poland syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:polymyalgia rheumatica n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:polymyalgia rheumatica | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:posterior fossa syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:posterior fossa syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:presentey anomaly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:prune belly syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:pseudohypoaldosteronism, type 1, recessive form n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:pulmonic stenosis and congenital nephrosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pulmonic stenosis and congenital nephrosis | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:pyle metaphyseal dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:pyramidal tract dysfunction n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pyramidal tract dysfunction | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:renal cysts and diabetes syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:renal cysts and diabetes syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:rud syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:rud syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:sarcosinemia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:smith-magenis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:somnolence syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:somnolence syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:spondylo-ocular syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:stickler syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:trichohepatoenteric syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:uveitis glaucoma and hyphema syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:uveitis glaucoma and hyphema syndrome | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> en:walker-warburg congenital muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:walker-warburg congenital muscular dystrophy | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 29 / 0.967 -> processus pathologique n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=processus pathologique | rel=r_associated | relid=0 | w=29 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> COL4A1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=COL4A1 | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:abstinence syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:abstinence syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:agyria (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:agyria (wws) | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:albinotic fundus n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:alpha-methylacyl-coa racemase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:angioma hereditary neurocutaneous n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:angioma hereditary neurocutaneous | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:ataxia, fatal x-linked, with deafness and loss of vision n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ataxia, fatal x-linked, with deafness and loss of vision | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:atypical hemolytic uremic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:atypical hemolytic uremic syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:autosomal recessive asexual dwarfism n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive asexual dwarfism | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:autosomal recessive distal osteolysis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:autosomal recessive inheritance n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:autosomal recessive spastic paraplegia type 11 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:beare-stevenson cutis gyrata syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:beta-aminoisobutyricaciduria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:beta-aminoisobutyricaciduria | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:brain iron accumulation type i syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:brain iron accumulation type i syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:cleft lip (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cleft lip (wws) | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:cod (cerebroocular dysgenesis) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cod (cerebroocular dysgenesis) | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:compartment syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:compartment syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:congenital adrenal hyperplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:congenital disorder of glycosylation type ia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:congenital varicella syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital varicella syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:crest syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:crest syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:crigler-najjar syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:deafness, progressive, with stapes fixation n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:deficiency of glucosyltransferase 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:dicarboxylicaminoaciduria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:diencephalic syndrome of infancy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:diencephalic syndrome of infancy | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:diffuse cerebral sclerosis of schilder n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:diffuse cerebral sclerosis of schilder | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:dilated ventricles (finding) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dilated ventricles (finding) | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:dry eye syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dry eye syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:duchenne muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:duchenne muscular dystrophy | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:dumping syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dumping syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:empty sella syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:episodic ataxia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:ethnologic n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ethnologic | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:evans syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:evans syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:exfoliation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:exfoliation syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:exposure as collected domain n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:exposure as collected domain | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:familial creutzfeldt-jakob n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:feingold syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:fronto-facio-nasal dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:geniospasm 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:gerstmann-straussler-scheinker disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:glutamate formiminotransferase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:glutathione synthetase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:hepatolenticular degeneration n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:hereditary factor xii deficiency disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary factor xii deficiency disease | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:histidinemia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:histidinemia | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:hnsha due to glutathione reductase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:hnsha due to glutathione synthetase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hnsha due to glutathione synthetase deficiency | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:hnsha due to pyrimidine-5'-nucleotidase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:hypokalemia, familial n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:hypoplasia of the brainstem n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypoplasia of the brainstem | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:kbg syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:kearns-sayre syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kearns-sayre syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:liddle syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:lupus anticoagulant disorder n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lupus anticoagulant disorder | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:marshall syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:marshall syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:meconium plug syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:meconium plug syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:meningoencephalocele (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:meningoencephalocele (wws) | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:miyoshi muscular dystrophy 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:miyoshi muscular dystrophy 1 | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:multiple system malformation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:multiple system malformation syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:muscle biopsy shows decreased glycosylation of alpha-dystroglycan (dag1, 128239) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscle biopsy shows decreased glycosylation of alpha-dystroglycan (dag1, 128239) | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:muscular dystrophy, oculopharyngeal n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy, oculopharyngeal | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:myopathy with exercise intolerance, swedish type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:neoplastic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neoplastic syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:netherton syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:neu-laxova syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neu-laxova syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:neuraminidase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:obstructive sleep apnea syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:obstructive sleep apnea syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:oculocerebral hypopigmentation syndrome type preus n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:oculodento-osseous dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:oculodento-osseous dysplasia | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:overgrowth syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:overgrowth syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:pallister-hall syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pallister-hall syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:papillon-lefevre syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:pathological aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pathological aspects | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:pomt1, 1-bp ins, 2110g n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pomt1, 1-bp ins, 2110g | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:pomt1, 3-bp del, 1260cct n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pomt1, 3-bp del, 1260cct | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:progeria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:progeria | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:progressive hemifacial atrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:progressive hemifacial atrophy | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:proteus syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:proteus syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:retinal dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:retinal dysplasia | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:retinal malformations (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:retinal malformations (wws) | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:rieger syndrome type 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:rieger syndrome type 1 | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:rna polymerase iii-related leukodystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:schinzel-giedion midface-retraction syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:severe childhood autosomal recessive muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:severe childhood autosomal recessive muscular dystrophy | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:severe muscular hypotonia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:severe muscular hypotonia | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:shwachman-diamond syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:shwachman-diamond syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:sonoda syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:spastic paraplegia 15, autosomal recessive n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:spondylocarpotarsal synostosis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:tarsal tunnel syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tarsal tunnel syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:teething syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:teething syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:tubulointerstitial nephritis and uveitis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tubulointerstitial nephritis and uveitis | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:upper limb defect with eye and ear abnormalities syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:uveomeningoencephalitic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:uveomeningoencephalitic syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:van der woude syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:van der woude syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:von hippel-lindau syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:von hippel-lindau syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:warsaw breakage syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:west syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:west syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:wolff-parkinson-white syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:wolff-parkinson-white syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> en:xyy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:xyy syndrome | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> GMPPB n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=GMPPB | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> hydrocéphalie n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=hydrocéphalie | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> POMT1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=POMT1 | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 28 / 0.933 -> Walker n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=Walker | rel=r_associated | relid=0 | w=28 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:acrocephalosyndactyly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acrocephalosyndactyly | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:antley-bixler syndrome, autosomal dominant n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:autosomal recessive scid n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:behcet syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:behcet syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:bloom syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:carbamoyl-phosphate synthetase i deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:cat-eye syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cat-eye syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0001) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0001) | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:central sleep apnea syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:central sleep apnea syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:cerebellar hypoplasia, severe (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebellar hypoplasia, severe (wws) | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:chemically induced n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chemically induced | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:chondrodysplasia punctata syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:chronic fatigue syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chronic fatigue syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:cockayne syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cockayne syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:complete or partial absence of the corpus callosum (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:complete or partial absence of the corpus callosum (wws) | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:congenital cataracts, facial dysmorphism, and neuropathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:congenital dyserythropoietic anemia, type i n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:congenital myasthenic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital myasthenic syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:connective and soft tissue n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:connective and soft tissue | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:diagnosis aspect n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:diagnosis aspect | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:disorder of central nervous system due to xeroderma pigmentosum n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:disorder of central nervous system due to xeroderma pigmentosum | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:dopa-responsive dystonia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:dyggve-melchior-clausen syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dyggve-melchior-clausen syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:dyskeratosis congenita, autosomal recessive n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:ehlers-danlos syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:ehlers-danlos syndrome, type vi n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ehlers-danlos syndrome, type vi | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:eisenmenger syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:eisenmenger syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:embryologic n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:embryologic | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:familial hemiplegic migraine n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:familial hypoaldosteronism n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:familial juvenile nephronophthisis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial juvenile nephronophthisis | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:fatty acid hydroxylase-associated neurodegeneration n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:felty syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:felty syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:fetal alcohol syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fetal alcohol syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:fetal warfarin syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fetal warfarin syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:fraser syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fraser syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:hecht syndrome (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hecht syndrome (disorder) | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:hereditary adrenal unresponsiveness to corticotropin n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:hereditary benign intraepithelial dyskeratosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:hereditary factor xi deficiency disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary factor xi deficiency disease | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:heterotaxy syndrome with polysplenia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:heterotaxy syndrome with polysplenia | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:holmes-adie syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:holmes-adie syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:hunter syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hunter syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:hyperprolinemia type 2 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:immunology aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:immunology aspects | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:jackson-weiss syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:kartagener syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kartagener syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:knuckle pads, leuconychia and sensorineural deafness n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:knuckle pads, leuconychia and sensorineural deafness | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:late-onset muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:late-onset muscular dystrophy | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:leber congenital amaurosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:leber congenital amaurosis | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:leukotriene c4 synthase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:lig4 syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lig4 syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:marles greenberg persaud syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:maroteaux-lamy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:melas syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:melas syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:melnick-fraser syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:mental retardation, profound (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mental retardation, profound (wws) | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:merosin-deficient congenital muscular dystrophy type 1a n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:merosin-deficient congenital muscular dystrophy type 1a | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:methylcrotonyl-coa carboxylase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:miller-dieker syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:miller-dieker syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:mmih syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:moloney syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:moloney syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:monosomy 13q syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:monosomy 13q syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:multiple organ failure n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:multiple organ failure | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:muscular dystrophies and other myopathies n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophies and other myopathies | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:muscular dystrophy, limb-girdle, type 2k n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy, limb-girdle, type 2k | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:myopia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:myopia | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:naxos disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:naxos disease | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:nephrotic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:nephrotic syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:neuroleptic malignant syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neuroleptic malignant syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:neutral lipid storage disease with myopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:oculo-respiratory syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:oculo-respiratory syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:oculocutaneous albinism type 4 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:onset prenatally or at birth n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:onset prenatally or at birth | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:otoonychoperoneal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:pachydermoperiostosis - familial n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pachydermoperiostosis - familial | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:pallister-killian syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pallister-killian syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:parasitology n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:parasitology | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:paroxysmal extreme pain disorder n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:pearson marrow-pancreas syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pearson marrow-pancreas syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:piriformis muscle syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:piriformis muscle syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:pomt1, 2-bp del, 2179tc n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pomt1, 2-bp del, 2179tc | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:pomt1, gly76arg n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pomt1, gly76arg | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:popliteal pterygium syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:primary hyperoxaluria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:rapadilino syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:retinitis punctata albescens (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:rett syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:rett syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:richards-rundle syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:severe disorder n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:severe disorder | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:shprintzen-goldberg craniosynostosis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:shprintzen-goldberg craniosynostosis syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:sjogren-larsson syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:soft tissue n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:soft tissue | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:substance withdrawal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:substance withdrawal syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:tooth and nail syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tooth and nail syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:tourette syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tourette syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:trichothiodystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:trichothiodystrophy | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:tyrosinemia, type iii n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:verloes bourguignon syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:virtually no active movement at birth (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:virtually no active movement at birth (wws) | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:waardenburg syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:waardenburg syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:waisman syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:werner syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:werner syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:wiskott-aldrich syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:wolman disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:wolman disease | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:x-linked emery-dreifuss muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:x-linked emery-dreifuss muscular dystrophy | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> en:xanthinuria, type i n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> LARGE n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=LARGE | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 27 / 0.9 -> syndrome de Chemke n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=syndrome de Chemke | rel=r_associated | relid=0 | w=27 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> cerveau n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=cerveau | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:1p36 deletion syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:1p36 deletion syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:adenylosuccinate lyase deficiency (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:adherence syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:adherence syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:adrenal gland hyperplasia ii n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:al awadi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:alpha-fetoprotein deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:amelogenesis imperfecta - recessive - rough n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:aminoacylase 1 deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:androgen insensitivity syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:androgen insensitivity syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:aniridia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aniridia | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:argininemia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:argininemia | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:atrophic retina n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:atrophic retina | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:autosomal dominant idiopathic familial dystonia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:autosomal recessive muscular dystrophy with limb girdle distribution n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:barth syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:barth syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:becker's muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:becker's muscular dystrophy | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:beckwith-wiedemann syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:brown-sequard syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:brown-sequard syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:brown-vialetto-van laere syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:burning mouth syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:burning mouth syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:carpal tunnel syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:carpal tunnel syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:cataract n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cataract | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:cerebellar ataxia, cayman type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:cerebral hemorrhage with amyloidosis, hereditary, dutch type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:cervicocranial syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cervicocranial syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:cobblestone lissencephaly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cobblestone lissencephaly | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:coffin-siris syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:coffin-siris syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:complete trisomy 18 syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:congenital muscular dystrophy-dystroglycanopathy with mental retardation type b2 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital muscular dystrophy-dystroglycanopathy with mental retardation type b2 | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:cytokine release syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cytokine release syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:de toni-debre-fanconi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:de toni-debre-fanconi syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:diarrhea-associated hemolytic uremic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:diarrhea-associated hemolytic uremic syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:diffuse infiltrative lymphocytosis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:diffuse infiltrative lymphocytosis syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:distal muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:distal muscular dystrophy | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:dravet syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dravet syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:duane syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:duane syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:etiology aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:etiology aspects | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:eye diseases, hereditary n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:eye diseases, hereditary | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:factor v and factor viii, combined deficiency of n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:fatal infantile lactic acidosis with methylmalonic aciduria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:fetal methotrexate syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fetal methotrexate syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:fetal retinoid syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fetal retinoid syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:game friedman paradice syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:game friedman paradice syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:glutamate-cysteine ligase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:glycine dehydrogenase (decarboxylating) deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:glycogen storage disease type i n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glycogen storage disease type i | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:glycogen storage disease type x n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:gurrieri sammito bellussi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hemolytic anemia due to pyruvate kinase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hereditary cerebral amyloid angiopathy, icelandic type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hereditary coproporphyria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary coproporphyria | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hereditary corneal dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary corneal dystrophy | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hereditary factor x deficiency disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hereditary fructose intolerance n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hereditary methemoglobinemia, enzymatic type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hereditary oculoleptomeningeal amyloid angiopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hermansky-pudlak syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hermansky-pudlak syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:heterotaxy syndrome with asplenia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:heterotaxy syndrome with asplenia | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hydrocephalus with cerebellar agenesis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hydrocephalus with cerebellar agenesis | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:hyperviscosity syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hyperviscosity syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:in cerebrospinal fluid n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:in cerebrospinal fluid | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:isaacs syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:klinefelter syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:korsakoff syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:korsakoff syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:landau-kleffner syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:landau-kleffner syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:leigh disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:leigh disease | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:lymphedema-distichiasis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lymphedema-distichiasis syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:macdermot winter syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:majority of wws patients die within the first year of life n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:majority of wws patients die within the first year of life | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:menopausal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:menopausal syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:methylene thf reductase deficiency and homocystinuria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:mobius syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:muscle-eye-brain disease, congenital muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscle-eye-brain disease, congenital muscular dystrophy | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 6 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 6 | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:muscular dystrophy-dystroglycanopathy (limb-girdle) type c, 5 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy-dystroglycanopathy (limb-girdle) type c, 5 | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:muscular dystrophy, congenital, with central nervous system involvement n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy, congenital, with central nervous system involvement | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:muscular dystrophy, scapulohumeral n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy, scapulohumeral | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:myopathy, early-onset, with fatal cardiomyopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:myotonic dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:myotonic dystrophy | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:neonatal research network terminology n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neonatal research network terminology | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:niemann-pick disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:oculomandibular dysostosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:oculomandibular dysostosis | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:orofaciodigital syndrome type 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:orofaciodigital syndrome type 1 | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:palmar-plantar erythodysthesia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:palmar-plantar erythodysthesia | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:pelizaeus merzbacher like disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:pena-shokeir syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pena-shokeir syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:peutz-jeghers syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:polymicrogyria (meb) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:polymicrogyria (meb) | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:prolonged electroretinal response suppression n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:psychology qualifier n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:psychology qualifier | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:renal dysplasia (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:renal dysplasia (wws) | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:scimitar syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:scimitar syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:sly syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sly syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:solitary median maxillary central incisor n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:solitary median maxillary central incisor | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:spinal muscular atrophy with respiratory distress 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:staphylococcal scalded skin syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:staphylococcal scalded skin syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:tay-sachs disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:thalidomide embryopathy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:thalidomide embryopathy syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:thyroid dyshormonogenesis 4 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:trichorhinophalangeal syndrome type ii n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:type a 14 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:type a 14 | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:ullrich congenital muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ullrich congenital muscular dystrophy | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:vertebral artery syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:vertebral artery syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:vitreoretinal dysgenesis (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:vitreoretinal dysgenesis (wws) | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:walker-warburg syndrome, fktn-related n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:walker-warburg syndrome, fktn-related | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:woodhouse sakati syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:woodhouse sakati syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:x-linked lissencephaly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:x-linked lissencephaly | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> en:yellow nail syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> oeil n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=oeil | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> protein O-mannosyl-transferases n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=protein O-mannosyl-transferases | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> syndrome de Walker-Warburg n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 26 / 0.867 -> syndrome de warburg n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=syndrome de warburg | rel=r_associated | relid=0 | w=26 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:2-hydroxyglutaric aciduria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:achenbach syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:achenbach syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:acquired hyperostosis syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acquired hyperostosis syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:alkaptonuria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:allgrove syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:alport syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alport syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:arthrogryposis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:atrophoderma vermiculatum n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:autoinflammatory syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autoinflammatory syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:autosomal dominant late onset basal ganglia degeneration n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal dominant late onset basal ganglia degeneration | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:blau syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:blau syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:buphthalmos (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:buphthalmos (wws) | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:cadasil syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:cerebellar cysts (meb) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebellar cysts (meb) | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:cerebellar mutism n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebellar mutism | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:cerebral cavernous malformation n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:childhood hypophosphatasia (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:choroideremia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:choroideremia | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:chromosome 15q11-q13 duplication syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chromosome 15q11-q13 duplication syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:chylomicron retention disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:complete trisomy 21 syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:complete trisomy 21 syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:congenital central hypoventilation n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital central hypoventilation | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:congenital contracture n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital contracture | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:congenital disorder of glycosylation type ic n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:congenital plasminogen activator inhibitor deficiency type 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:cowden syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cowden syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:de barsy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:de barsy syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:deficiency of fructokinase n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:deficiency of fructokinase | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:diabetes mellitus, insulin-resistant, with acanthosis nigricans n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:diabetes mellitus, insulin-resistant, with acanthosis nigricans | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:dubowitz syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dubowitz syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:dysfunctional elimination syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dysfunctional elimination syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:epidermolysis bullosa simplex with pyloric atresia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:epiphyseal dysplasia, multiple, 4 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:familial acantholysis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:familial benign neonatal epilepsy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:fanconi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fanconi syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:fatal familial insomnia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:gamma-glutamyltransferase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:genetic heterogeneity n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:genetic heterogeneity | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:gray baby syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gray baby syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:hallermann syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hallermann syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:hereditary motor neuron disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary motor neuron disease | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:hnsha due to diphosphoglycerate mutase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:holt-oram syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:hurler syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hurler syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:hurler-scheie syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hurler-scheie syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:hypophosphatemic rickets with hypercalciuria, hereditary n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:infantile convulsions and paroxysmal choreoathetosis, familial n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:infantile convulsions and paroxysmal choreoathetosis, familial | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:insufficient breast milk syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:insufficient breast milk syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:loeys-dietz syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:loffler syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:loffler syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:mandibuloacral dysplasia with type a lipodystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:microcephaly-capillary malformation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:miliaria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:miliaria | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:mulibrey nanism n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mulibrey nanism | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:multiple sulfatase deficiency disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 1 | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:neuronal intranuclear inclusion disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neuronal intranuclear inclusion disease | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:norrie syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:odontohypophosphatasia (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:opitz g/bbb syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:opitz g/bbb syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:periventricular heterotopia, x-linked n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:periventricular heterotopia, x-linked | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:pettigrew syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pettigrew syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:pituitary thyroid hormone resistance n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pituitary thyroid hormone resistance | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:pomt1, 1-bp dup, 2167g n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pomt1, 1-bp dup, 2167g | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:pontocerebellar hypoplasia type 2 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:post-pericardiotomy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:post-pericardiotomy syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:radiation sickness syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:radiation sickness syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:red man syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:red man syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:rehabilitation aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:rehabilitation aspects | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:renal tubular acidosis, distal, with progressive nerve deafness n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:renal tubular acidosis, distal, with progressive nerve deafness | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:renal tubulopathy with encephalopathy and liver failure syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:saito kuba tsuruta syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:septo-optic dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:septo-optic dysplasia | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:spondyloenchondrodysplasia with immune dysregulation n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:spondyloepiphyseal dysplasia, omani type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:sudden infant death syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sudden infant death syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:sunct syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sunct syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:sunset syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sunset syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:syndrome of apparent mineralocorticoid excess n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:tolosa-hunt syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tolosa-hunt syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:tuberous sclerosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:twiddler's syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:twiddler's syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:usher syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:usher syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:vascular access steal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:vascular access steal syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:virtual absence of pyramidal tracts (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:virtual absence of pyramidal tracts (wws) | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:western type of congenital muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:western type of congenital muscular dystrophy | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:xeroderma pigmentosum n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> en:zollinger ellison syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:zollinger ellison syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> encéphale n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=encéphale | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> FKRP gene n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=FKRP gene | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> génétique n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=génétique | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> hard syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=hard syndrome | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> maladie génétique n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=maladie génétique | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> maladie neuro-musculaire héréditaire n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=maladie neuro-musculaire héréditaire | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> maladies n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=maladies | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> maladies génétiques n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=maladies génétiques | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> médecine n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=médecine | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> myopathie n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=myopathie | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> POMGnT1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=POMGnT1 | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> POMT2 gen e n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=POMT2 gen e | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 25 / 0.833 -> Walker-Warburg (syndrome de) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=25 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> agyrie n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=agyrie | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:5-oxoprolinase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:5' 10' methylenetetrahydrofolate reductase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:acquired immunodeficiency syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acquired immunodeficiency syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:acrocallosal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:alagille syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:allan-herndon-dudley syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:alstrom syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:andersen syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:anemia, hypochromic microcytic, with iron overload n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:angelman syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:apl differentiation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:apl differentiation syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:aspects of mortality statistics n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aspects of mortality statistics | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:aspects of radionuclide imaging n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aspects of radionuclide imaging | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:autosomal recessive primary microcephaly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:autosomal recessive sideroblastic anemia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:bietti crystalline corneoretinal dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:bile acid synthesis defect n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bile acid synthesis defect | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:bone n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bone | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:bonnevie-ullrich syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bonnevie-ullrich syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:bothnia retinal dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:cartilage hair hypoplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cartilage hair hypoplasia | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:cerebral lipidosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebral lipidosis | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:cerebrooculofacioskeletal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebrooculofacioskeletal syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:chitty hall baraitser syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:cleidocranial dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:cogan-reese syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cogan-reese syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:complication aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:complication aspects | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:congenital hereditary muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital hereditary muscular dystrophy | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:congenital muscular dystrophy (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital muscular dystrophy (disorder) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:congenital nephrogenic diabetes insipidus n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:corneal haze n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:corneal haze | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:cushing syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cushing syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:cystic fibrosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cystic fibrosis | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:dialyzer first use syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dialyzer first use syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:dihydrouracil dehydrogenase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dihydrouracil dehydrogenase deficiency | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:dyskeratosis congenita n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dyskeratosis congenita | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:dystroglycans n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dystroglycans | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:ear, patella, short stature syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:endocrine syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:endocrine syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:episodic pain syndrome, familial, 3 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:episodic pain syndrome, familial, 3 | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:fetal hydantoin syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fetal hydantoin syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:fibromyalgia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fibromyalgia | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:fibular hypoplasia and complex brachydactyly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:frontotemporal dementia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:fryns macrocephaly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:giacci familial neurogenic acroosteolysis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:gilbert syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gilbert syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:gitelman syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gitelman syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:hair tourniquet n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hair tourniquet | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:hellp syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hellp syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:hereditary peripheral neuropathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary peripheral neuropathy | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:herrmann syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:herrmann syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:historical aspects qualifier n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:historical aspects qualifier | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:hydrocephalus n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hydrocephalus | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:hypereosinophilic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypereosinophilic syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:hyperphosphatasia with mental retardation n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:in blood n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:in blood | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:in urine n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:in urine | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:infantile globoid cell leukodystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:inherited metabolic disorder of nervous system n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:inherited metabolic disorder of nervous system | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:intestinal epithelial dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:isovaleric acidemia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:jervell and lange nielsen syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:knobloch syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:laron syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:laron syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:leriche syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:leriche syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:lethal congenital contracture syndrome 2 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:lethal multiple pterygium syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lethal multiple pterygium syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:li-fraumeni syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:macrophage activation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:macrophage activation syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:macular corneal dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:majeed syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:malabsorption syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:malabsorption syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:megalocornea (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:megalocornea (wws) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:melkersson-rosenthal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:melkersson-rosenthal syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:metabolic aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:metabolic aspects | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:microcephaly, amish type (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:microphthalmia (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microphthalmia (wws) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:microtia (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microtia (wws) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:miller-mckusick-malvaux-syndrome (3m syndrome) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:morquio syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:mousa al din al nassar syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mousa al din al nassar syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:mucociliary clearance defect n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mucociliary clearance defect | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:multiple endocrine neoplasia type 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:multiple endocrine neoplasia type 1 | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:nail-patella syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:neuroacanthocytosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:neurodegeneration due to cerebral folate transport deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:northern epilepsy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:nutritional management n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:nutritional management | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:orofaciodigital syndrome type 6 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:orofaciodigital syndrome type 6 | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:pain amplification syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pain amplification syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:persistent mullerian duct syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:phenylketonuria ii n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:physiopathological n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:physiopathological | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:posterior fossa cysts (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:posterior fossa cysts (wws) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:potocki-shaffer syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:premenstrual syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:premenstrual syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:pseudotrisomy 13 syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:purine-nucleoside phosphorylase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:renal coloboma syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:renal coloboma syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:retinal dysplasia (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:retinal dysplasia (wws) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:reye syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:reye syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:selective antibody deficiency with normal immunoglobulins n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:selective antibody deficiency with normal immunoglobulins | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:shone syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:shone syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:sick sinus syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sick sinus syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:sinus histiocytosis with massive lymphadenopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sinus histiocytosis with massive lymphadenopathy | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:stein-leventhal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:stein-leventhal syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:stokes-adams syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:stokes-adams syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:succinic semialdehyde dehydrogenase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:susac syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:susac syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:tetra-amelia autosomal recessive n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tetra-amelia autosomal recessive | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:thin cortical mantle (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:thin cortical mantle (wws) | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:thyroid associated opthalmopathies n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:thyroid associated opthalmopathies | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:torch syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:torch syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:townes-brocks syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:townes-brocks syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:urocanase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:valinemia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:valinemia | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:vitelliform macular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:waardenburg syndrome type 4 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:waardenburg syndrome type 4 | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:xxxy and xxxxy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:xxxy and xxxxy syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> en:zellweger syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=syndrome | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> syndrome de n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=syndrome de | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 24 / 0.8 -> Warburg n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=Warburg | rel=r_associated | relid=0 | w=24 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:3-methylglutaconic aciduria type 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:3-methylglutaconic aciduria type 1 | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:acroparesthesia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acroparesthesia syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:acute coronary syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acute coronary syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:acute respiratory distress syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acute respiratory distress syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:alpha thalassemia x-linked mental retardation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alpha thalassemia x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:amelogenesis imperfecta nephrocalcinosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:amelogenesis imperfecta nephrocalcinosis | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:amniotic band syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:arakawa syndrome ii n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:argininosuccinic aciduria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:autosomal recessive idiopathic familial dystonia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:bangstad syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bangstad syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:bannayan syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bannayan syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:bardet-biedl syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:basal ganglia disease, biotin-responsive n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:basilar artery syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:basilar artery syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:bernard-soulier syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bernard-soulier syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:blindness (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:blindness (wws) | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:bowen-conradi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:cerebellar dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebellar dysplasia | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:cerebrotendinous xanthomatosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:charcot-marie-tooth disease type 4 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:charge syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:charge syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:childhood myocerebrohepatopathy spectrum n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:chromosome 2q37 deletion syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chromosome 2q37 deletion syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:chronic progressive external ophthalmoplegia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:chronic progressive external ophthalmoplegia | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:churg-strauss syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:churg-strauss syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:classical phenylketonuria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:cleft lip/palate-ectodermal dysplasia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:codas syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:codas syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:complete trisomy 13 syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:complete trisomy 13 syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:congenital abnormality n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:congenital alpha-2-antiplasmin deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:congenital amegakaryocytic thrombocytopenia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:congenital bowing of long bone n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:congenital cerebellar hypoplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital cerebellar hypoplasia | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:corpus callosum agenesis neuronopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:desmosterolosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:down syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:down syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:dubin-johnson syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:ectodermal dysplasia/ skin fragility syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:emery-dreifuss muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:emery-dreifuss muscular dystrophy | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:exophthalmia (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:exophthalmia (wws) | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:familial encephalopathy with neuroserpin inclusion bodies n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:familial renal iminoglycinuria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:fisher syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fisher syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:fragile x tremor/ataxia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fragile x tremor/ataxia syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:frontotemporal dementia, chromosome 3-linked n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:gaze palsy, familial horizontal, with progressive scoliosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:generalized epilepsy and paroxysmal dyskinesia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:genetic aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:genetic aspects | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:goodpasture syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:goodpasture syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:gorlin chaudhry moss syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gorlin chaudhry moss syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:hajdu-cheney syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hajdu-cheney syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:hereditary cerebellar atrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary cerebellar atrophy | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:hereditary cystatin c amyloid angiopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:hereditary neuraxial edema n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary neuraxial edema | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:hereditary palmoplantar keratoderma gamborg nielsen type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:holoprosencephaly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:horner syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:horner syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:hypomagnesemia 1, intestinal n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:incontinentia pigmenti n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:incontinentia pigmenti | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:interleukin-1 receptor-associated kinase 4 deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:irritable bowel syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:irritable bowel syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:isolated hyperchlorhidrosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:joubert syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:left ventricular non-compaction syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:left ventricular non-compaction syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:lissencephaly syndrome, norman-roberts type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:malignant hyperthermia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:malignant hyperthermia syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:mannosidosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mannosidosis | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:maternally inherited mitochondrial dystonia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:maternally inherited mitochondrial dystonia | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:mayer-rokitansky-kuster-hauser syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mayer-rokitansky-kuster-hauser syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:medium-chain acyl-coa dehydrogenase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:microcephaly cervical spine fusion anomalies n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:mowat-wilson syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:multisystem disorder n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:multisystem disorder | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:muscle eye brain disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscle eye brain disease | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:neurofibromatosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neurofibromatosis | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:occipital encephalocele (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:occipital encephalocele (wws) | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:orofacial cleft 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:orofacial cleft 1 | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:parinaud syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:parinaud syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:pediatric terminology n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pediatric terminology | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:perinatal blood aspiration syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:perinatal blood aspiration syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:peters anomaly (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:peters anomaly (wws) | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:pierre robin syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pierre robin syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:pomt1, 3-bp del, 418atg n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pomt1, 3-bp del, 418atg | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:pre-excitation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pre-excitation syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:pseudocholinesterase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:rigid spine muscular dystrophy 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:rigid spine muscular dystrophy 1 | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:robinow syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:royers syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:royers syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:sea-blue histiocyte syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sea-blue histiocyte syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:sheehan syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sheehan syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:shy-drager syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:shy-drager syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:spondyloenchondromatosis with basal ganglia calcification n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spondyloenchondromatosis with basal ganglia calcification | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:spondyloepiphyseal dysplasia tarda, toledo type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:superior mesenteric artery syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:superior mesenteric artery syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:systemic inflammatory response syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:systemic inflammatory response syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:tempi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tempi syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:toxic shock syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:toxic shock syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:treacher collins syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:triploidy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:triploidy syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:walker-warburg syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:werdnig-hoffmann disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:werdnig-hoffmann disease | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> en:williams syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:williams syndrome | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 23 / 0.767 -> Fukuyama (dystrophie musculaire de) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=Fukuyama (dystrophie musculaire de) | rel=r_associated | relid=0 | w=23 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> Dandy-Walker (syndrome) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=Dandy-Walker (syndrome) | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:3-methylglutaconic aciduria type iv n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:adenine phosphoribosyltransferase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:aortic arch syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aortic arch syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:arterial tortuosity syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:aspartylglycosaminuria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:benign congenital myopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:benign congenital myopathy | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:borjeson-forssman-lehmann syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:borjeson-forssman-lehmann syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:cauda equina syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cauda equina syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:cerebellar ataxia ectodermal dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:cleft palate (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cleft palate (wws) | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:combined malonic and methylmalonic aciduria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:congenital leptin deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:congenital transferrin deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:costello syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:costello syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:craniodiaphyseal dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:craniofacial deafness hand syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:craniofacial deafness hand syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:creatine phosphokinase serum increased n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:creatine phosphokinase serum increased | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:dandy-walker malformation (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dandy-walker malformation (wws) | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:diethylstilbestrol syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:diethylstilbestrol syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:donnai-barrow syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:dystonia 12 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dystrophy | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:ellis-van creveld syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ellis-van creveld syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:enterokinase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:epidemiologic n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:epidemiologic | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:ethanolaminosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:facioscapulohumeral muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:facioscapulohumeral muscular dystrophy | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:female restricted epilepsy with intellectual disability syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:female restricted epilepsy with intellectual disability syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:flattening of the pons n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:flattening of the pons | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:frohlich syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:frohlich syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:fryns syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fryns syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:fucosidosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fucosidosis | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:gasping syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gasping syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:glycogen storage disease type vii n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:glycogen storage disease type vii | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:gray platelet syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gray platelet syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:guillain-barre syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:guillain-barre syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:hantavirus pulmonary syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hantavirus pulmonary syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:hereditary cerebellar degeneration n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary cerebellar degeneration | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:hereditary spastic paralysis, infantile onset ascending n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:heterotaxy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:hnsha due to glucose phosphate isomerase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hnsha due to glucose phosphate isomerase deficiency | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:hyperimmunoglobulin e syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hyperimmunoglobulin e syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:hyperprolinemia type 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:iridocorneal endothelial syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:iridocorneal endothelial syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:jankovic rivera syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:juvenile x-linked retinoschisis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:klein-waardenberg's syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:klein-waardenberg's syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:klippel-feil syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:leopard syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:lipase hypersecretion syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lipase hypersecretion syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:lubs x-linked mental retardation syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:maple syrup urine disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:marinesco-sjogren syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:marinesco-sjogren syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:maternal uniparental disomy chromosome 14 syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:maternal uniparental disomy chromosome 14 syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:meconium aspiration syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:meconium aspiration syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:megalencephalic leukoencephalopathy with subcortical cysts n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:menkes disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:menkes disease | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:mental retardation, severe (meb) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mental retardation, severe (meb) | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:metabolic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:metabolic syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:methylmalonyl-coenzyme a mutase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:microcephalic primordial dwarfism toriello type n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:moderate steroid 21-hydroxylase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:mucopolysaccharidosis type i n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:muenke syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muenke syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:multicentric osteolysis, nodulosis, and arthropathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:multicentric osteolysis, nodulosis, and arthropathy | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:muscular dystrophy not predominantly limb girdle in distribution n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy not predominantly limb girdle in distribution | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 2 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 2 | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:myhre syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:n-acetylglutamate synthase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:nathalie syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:north american indian childhood cirrhosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:patients with meb have less severe features and longer survival n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:patients with meb have less severe features and longer survival | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:pelvic muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pelvic muscular dystrophy | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:phenotypic variability n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:phenotypic variability | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:plummer-vinson syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:plummer-vinson syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:potter syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:potter syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:prickle1-related progressive myoclonus epilepsy with ataxia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:propionic acidemia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:proteus-like syndrome (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:reardon hall slaney syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:renal dysplasia and retinal aplasia (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:renal dysplasia and retinal aplasia (disorder) | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:restless leg syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:restless leg syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:retinal detachment (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:retinal detachment (wws) | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:retinitis pigmentosa n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:retinitis pigmentosa | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:reversible posterior leukoencephalopathy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:reversible posterior leukoencephalopathy syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:salcedo syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:salcedo syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:sarcoidosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sarcoidosis | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:scheie syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:scheie syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:schwartz-jampel syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:schwartz-jampel syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:seizure n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:seizure | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:short bowel syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:short bowel syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:short rib-polydactyly syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:short rib-polydactyly syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:sicca syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sicca syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:sick euthyroid syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sick euthyroid syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:sitosterolemia with xanthomatosis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:spinocerebellar ataxia with epilepsy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:spinocerebellar ataxia, autosomal recessive 2 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:sudden infant death with dysgenesis of the testes syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:sweet syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sweet syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:swyer james syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:swyer james syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:synpolydactyly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:telomeric 22q13 monosomy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:telomeric 22q13 monosomy syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:therapeutic aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:therapeutic aspects | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:thiamine responsive megaloblastic anemia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:thiamine responsive megaloblastic anemia syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:thomas syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:trichorhinophalangeal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:trichorhinophalangeal syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:tyrosinemia type ii n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:vacterl association n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:vacterl association | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:viruses n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:viruses | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:waardenburg anophthalmia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:weill-marchesani syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:weill-marchesani syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:x-linked epilepsy with learning disability and behavior disorder syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:x-linked epilepsy with learning disability and behavior disorder syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> en:xxxy syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:xxxy syndrome | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> FKTN gene n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=FKTN gene | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> ISPD n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=ISPD | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 22 / 0.733 -> LARGE1 gene n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=LARGE1 gene | rel=r_associated | relid=0 | w=22 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> dystrophie musculaire congénitale n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=dystrophie musculaire congénitale | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:absent auditory canals (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:absent auditory canals (wws) | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:acrodermatitis enteropathica n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:acromegaly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:acromegaly | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:albright's hereditary osteodystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:albright's hereditary osteodystrophy | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:allanson pantzar mcleod syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:allanson pantzar mcleod syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:alper syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:alper syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:aredyld syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:aredyld syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:autosomal recessive ocular albinism n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:baller-gerold syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:barrett esophagus n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:barrett esophagus | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:bartter syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:bartter syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:behavioral variant of frontotemporal dementia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:behrens baumann dust syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:calciphylaxis n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:calciphylaxis | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:capgras syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:capgras syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:capillary leak syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:capillary leak syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:carbohydrate-deficient glycoprotein syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:carbohydrate-deficient glycoprotein syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:cohen syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:combined pituitary hormone deficiency genetic form n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:combined pituitary hormone deficiency genetic form | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:complex regional pain syndrome i n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:complex regional pain syndrome i | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:complex regional pain syndrome ii n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:complex regional pain syndrome ii | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:cri du chat syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:cryopyrin-associated periodic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cryopyrin-associated periodic syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:cystathionine beta-synthase deficiency disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:dandy-walker malformation n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:dandy-walker malformation | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:digeorge syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:ectodermal dysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:enzymology n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:enzymology | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:epilepsy, myoclonic, benign adult familial, type 2 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:fetal valproate syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fetal valproate syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:foxg1 syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:fragile x syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:freeman-sheldon syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:fructose-1,6-bisphosphatase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:goldenhar syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:gracile syndrome (disorder) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:greig syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:greig syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:hmg-coa lyase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:hypomyelination and congenital cataract n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:hypoplastic genitalia (wws) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:hypoplastic genitalia (wws) | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:i-cell disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:i-cell disease | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:inspissated bile syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:inspissated bile syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:iris coloboma with ptosis, hypertelorism, and mental retardation n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:iris coloboma with ptosis, hypertelorism, and mental retardation | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:jacobsen syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:kleine-levin syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kleine-levin syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:klippel-trenaunay-weber syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:kuskokwim disease n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:lactase deficiency, congenital n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:lecithin acyltransferase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:lennox-gastaut syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lennox-gastaut syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:lethal congenital contracture syndrome 1 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:lethal congenital contracture syndrome type 3 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:lipodystrophy, partial, with rieger anomaly, short stature, and insulinopenic diabetes mellitus n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lipodystrophy, partial, with rieger anomaly, short stature, and insulinopenic diabetes mellitus | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:lipoprotein glomerulopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:lipoprotein glomerulopathy | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:melanoma astrocytoma syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:microbiological n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microbiological | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:mitochondrial dna depletion syndrome 2 (myopathic type) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:mohr-tranebjaerg syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:multicentric osteolysis nodulosis arthropathy spectrum n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 3 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 3 | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:nelson syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:nelson syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:neonatal progeroid syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:neurodegeneration with brain iron accumulation 4 n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:nonaka myopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:noonan syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:oculopharyngeal muscular dystrophy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:oculopharyngeal muscular dystrophy | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:okihiro syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:pancreatic triacylglycerol lipase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:pentosuria n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pentosuria | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:periodic fever syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:periodic fever syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:peters-plus syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:pili torti-deafness syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pili torti-deafness syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:pituitary stalk interruption syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pituitary stalk interruption syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:pomt1, gln303ter n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:pomt1, gln303ter | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:porphobilinogen synthase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:postural orthostatic tachycardia syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:postural orthostatic tachycardia syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:prader-willi habitus, osteopenia, and camptodactyly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:prader-willi syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:prolidase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:rabson mendenhall syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:rabson mendenhall syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:reiter syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:reiter syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:respiratory distress syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:respiratory distress syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:roberts syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:russell-silver syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:sanfilippo syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:schindler disease, type i n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:schindler disease, type i | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:seckel syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:seckel syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:sotos syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:spondyloenchondrodysplasia n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:subclavian steal syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:subclavian steal syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:sulfite oxidase deficiency n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:superior vena cava syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:superior vena cava syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:surgical aspects n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:surgical aspects | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:temporomandibular joint dysfunction syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:temporomandibular joint dysfunction syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:tethered spinal cord syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tethered spinal cord syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:thoracic outlet syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:thoracic outlet syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:tricho-thiodystrophy disorder n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tricho-thiodystrophy disorder | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:trichorhinophalangeal syndrome type i n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:trichorhinophalangeal syndrome type i | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:tungland bellman syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:turner syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:turner syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:type ii acrocephalopolysyndactyly n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:use of ultrasonography n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:use of ultrasonography | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:uv-sensitive syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:wells jankovic syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:wells jankovic syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:wernicke-korsakoff syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:wernicke-korsakoff syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:wolfram syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:wolfram syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:x-linked dystonia parkinsonism n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:x-linked dystonia parkinsonism | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> en:x-linked hydrocephalus syndrome n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:x-linked hydrocephalus syndrome | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> FKRP n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=FKRP | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> FKTN n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=FKTN | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> lissencéphalie n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=lissencéphalie | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 21 / 0.7 -> POMT1 gene n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=POMT1 gene | rel=r_associated | relid=0 | w=21 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 15 / 0.5 -> maladie du muscle n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=maladie du muscle | rel=r_associated | relid=0 | w=15 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 15 / 0.5 -> maladie musculaire n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=maladie musculaire | rel=r_associated | relid=0 | w=15 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 15 / 0.5 -> Maladies génétiques n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=Maladies génétiques | rel=r_associated | relid=0 | w=15 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 15 / 0.5 -> myopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=myopathy | rel=r_associated | relid=0 | w=15 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 10 / 0.333 -> Walker-Warburg n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=Walker-Warburg | rel=r_associated | relid=0 | w=10 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 5 / 0.167 -> en:myopathy n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:myopathy | rel=r_associated | relid=0 | w=5 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) -- r_associated #0: 5 / 0.167 -> maladies héréditaires n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=maladies héréditaires | rel=r_associated | relid=0 | w=5

≈ 610 relations entrantes syndrome de Walker-Warburg --- r_associated #0: 42 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Walker-Warburg | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=42 Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=Walker-Warburg (syndrome de) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=40 en:walker-warburg syndrome --- r_associated #0: 25 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:walker-warburg syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=25 en:type a 14 --- r_associated #0: 21 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:type a 14 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=21 œil --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=œil | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 COL4A1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=COL4A1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 GMPPB --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=GMPPB | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 LARGE --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=LARGE | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 POMT1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=POMT1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 Walker --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=Walker | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 cerveau --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=cerveau | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 dysplasie olfacto-génitale --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=dysplasie olfacto-génitale | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 dysplasie olfactogénitale --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=dysplasie olfactogénitale | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=dysplasie olfactogénitale de De Morsier | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 dystroglycanopathies --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=dystroglycanopathies | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:17q21 microdeletion syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:17q21 microdeletion syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:1p36 deletion syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:1p36 deletion syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:21-hydroxylase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:21-hydroxylase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:22q telomere deletion syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:22q telomere deletion syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:3-methylglutaconic aciduria type 3 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:3-methylglutaconic aciduria type 3 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:3-methylglutaconic aciduria type 5 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:3-methylglutaconic aciduria type 5 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:5 alpha steroid reductase 2 deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:aagenaes syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:aagenaes syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:abstinence syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:abstinence syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:achard syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:achard syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:acid phosphatase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:acid phosphatase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:acrocephalosyndactyly --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:acrocephalosyndactyly | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:adherence syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:adherence syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:adrenal gland hyperplasia ii --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:adrenal gland hyperplasia ii | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:agyria (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:agyria (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:aicardi syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:aicardi syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:al awadi syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:al awadi syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:albinism --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:albinism | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:albinotic fundus --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:albinotic fundus | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:alice in wonderland syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:alice in wonderland syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:alpha dystroglycanopathies --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:alpha dystroglycanopathies | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:alpha, alpha-trehalase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:alpha, alpha-trehalase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:alpha-1 antitrypsin deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:alpha-1 antitrypsin deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:alpha-fetoprotein deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:alpha-fetoprotein deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:amelogenesis imperfecta - recessive - rough --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:amelogenesis imperfecta - recessive - rough | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:aminoacylase 1 deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:aminoacylase 1 deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:aminomethyltransferase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:aminomethyltransferase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:androgen insensitivity syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:androgen insensitivity syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:angioma hereditary neurocutaneous --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:angioma hereditary neurocutaneous | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:aniridia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:aniridia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:anterior chamber malformation (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:anterior chamber malformation (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:antiphospholipid syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:antiphospholipid syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:antley-bixler syndrome, autosomal dominant | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:arginine:glycine amidinotransferase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:arginine:glycine amidinotransferase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:argininemia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:argininemia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ataxia telangiectasia syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ataxia telangiectasia syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ataxia with vitamin e deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ataxia with vitamin e deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ataxia, fatal x-linked, with deafness and loss of vision --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ataxia, fatal x-linked, with deafness and loss of vision | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ateliotic dwarfism without insulinopenia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ateliotic dwarfism without insulinopenia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:atrophic retina --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:atrophic retina | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:atypical hemolytic uremic syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:atypical hemolytic uremic syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:autoinflammation, lipodystrophy and dermatosis syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:autoinflammation, lipodystrophy and dermatosis syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:autosomal dominant idiopathic familial dystonia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:autosomal dominant idiopathic familial dystonia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:autosomal recessive asexual dwarfism --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:autosomal recessive asexual dwarfism | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:autosomal recessive distal osteolysis syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:autosomal recessive ichthyosis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:autosomal recessive ichthyosis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:autosomal recessive inheritance --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:autosomal recessive inheritance | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:autosomal recessive scid --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:autosomal recessive scid | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:autosomal recessive spastic paraplegia type 11 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:autosomal recessive spastic paraplegia type 11 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ayala's disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ayala's disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:barth syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:barth syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:beare-stevenson cutis gyrata syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:becker generalized myotonia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:becker generalized myotonia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:becker's muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:becker's muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:beckwith-wiedemann syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:beckwith-wiedemann syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:behcet syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:behcet syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:behr syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:behr syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:beta-aminoisobutyricaciduria --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:beta-aminoisobutyricaciduria | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:biotinidase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:biotinidase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:bloom syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:bloom syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:brachydactyly syndrome type b --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:brachydactyly syndrome type b | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:brain iron accumulation type i syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:brain iron accumulation type i syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:brody myopathy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:brody myopathy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:brown-sequard syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:brown-sequard syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:brown-vialetto-van laere syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:brown-vialetto-van laere syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:burning mouth syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:burning mouth syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:camurati-engelmann syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:camurati-engelmann syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cardio-facio-cutaneous syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cardio-facio-cutaneous syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cardiofaciocutaneous syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cardiofaciocutaneous syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cardiorenal syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cardiorenal syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:carpal tunnel syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:carpal tunnel syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cat-eye syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cat-eye syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cataract --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cataract | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0001) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:caused by mutation in the protein o-mannosyltransferase-1 gene (pomt1, 607423.0001) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:central sleep apnea syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:central sleep apnea syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia, cayman type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cerebellar ataxia, cayman type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cerebellar hypoplasia, severe (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cerebellar hypoplasia, severe (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cerebral hemorrhage with amyloidosis, hereditary, dutch type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cervicocranial syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cervicocranial syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:chediak-higashi syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:chediak-higashi syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:chemically induced --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:chemically induced | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:chondrodysplasia punctata syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:chondrodysplasia punctata syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:choreoathetosis/spasticity, episodic --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:choreoathetosis/spasticity, episodic | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:chromosome 16p11.2 deletion syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:chromosome 16p11.2 deletion syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:chronic fatigue syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:chronic fatigue syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:chronic infantile neurological cutaneous and articular syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:chronic infantile neurological cutaneous and articular syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:citrin deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:citrin deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cleft lip (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cleft lip (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cobblestone lissencephaly --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cobblestone lissencephaly | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cobblestone lissencephaly, type ii (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cobblestone lissencephaly, type ii (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cockayne syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cockayne syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cod (cerebroocular dysgenesis) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cod (cerebroocular dysgenesis) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:coffin-lowry syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:coffin-lowry syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:coffin-siris syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:coffin-siris syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:coloboma (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:coloboma (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:compartment syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:compartment syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:complete or partial absence of the corpus callosum (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:complete or partial absence of the corpus callosum (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:complete trisomy 18 syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:complete trisomy 18 syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital adrenal hyperplasia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital adrenal hyperplasia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation type ia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital disorder of glycosylation type ia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital disorder of glycosylation type ig --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital disorder of glycosylation type ig | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital dyserythropoietic anemia, type i --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital dyserythropoietic anemia, type i | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital dyserythropoietic anemia, type ii | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital malformation syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital malformation syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital muscular dystrophy with arthrogryposis multiplex congenita --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital muscular dystrophy with arthrogryposis multiplex congenita | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital muscular dystrophy-dystroglycanopathy with mental retardation type b2 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital muscular dystrophy-dystroglycanopathy with mental retardation type b2 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital myasthenic syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital myasthenic syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital pancreatic enterokinase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital pancreatic enterokinase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital sucrase-isomaltase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital sucrase-isomaltase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:congenital varicella syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:congenital varicella syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:conn syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:conn syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:connective and soft tissue --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:connective and soft tissue | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:crest syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:crest syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:crigler-najjar syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:crigler-najjar syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:crisponi syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:crisponi syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cryptophthalmos syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cryptophthalmos syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cutis laxa, autosomal recessive --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cutis laxa, autosomal recessive | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cystinosis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cystinosis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cytochrome-c oxidase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cytochrome-c oxidase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:cytokine release syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cytokine release syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:de sanctis-cacchione syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:de sanctis-cacchione syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:de toni-debre-fanconi syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:de toni-debre-fanconi syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:deafness, progressive, with stapes fixation --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:deafness, progressive, with stapes fixation | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:deafness, sensorineural, and male infertility --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:deafness, sensorineural, and male infertility | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:deficiency of glucosyltransferase 1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:deficiency of glucosyltransferase 1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:deletion 18p syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:deletion 18p syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:deletion 18q syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:deletion 18q syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:dentatorubral-pallidoluysian atrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:diagnosis aspect --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:diagnosis aspect | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:diarrhea-associated hemolytic uremic syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:diarrhea-associated hemolytic uremic syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:dicarboxylicaminoaciduria --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:dicarboxylicaminoaciduria | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:diencephalic syndrome of infancy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:diencephalic syndrome of infancy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:diffuse cerebral sclerosis of schilder --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:diffuse cerebral sclerosis of schilder | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:diffuse infiltrative lymphocytosis syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:diffuse infiltrative lymphocytosis syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:dilated ventricles (finding) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:dilated ventricles (finding) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:disorder of central nervous system due to xeroderma pigmentosum --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:disorder of central nervous system due to xeroderma pigmentosum | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:disorganized brain cytoarchitecture --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:disorganized brain cytoarchitecture | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:distal muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:distal muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:donohue syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:donohue syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:dopa-responsive dystonia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:dopa-responsive dystonia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:double cortex syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:double cortex syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:dravet syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:dravet syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:drug hypersensitivity syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:drug hypersensitivity syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:dry eye syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:dry eye syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:duane syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:duane syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:duchenne muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:duchenne muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:dumping syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:dumping syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:dyggve-melchior-clausen syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:dyggve-melchior-clausen syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:dyskeratosis congenita, autosomal recessive | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ectrodactyly --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ectrodactyly | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ehlers-danlos syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, arthrochalasia type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ehlers-danlos syndrome, arthrochalasia type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, type vi --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ehlers-danlos syndrome, type vi | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:eisenmenger syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:eisenmenger syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:embryologic --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:embryologic | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:empty sella syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:empty sella syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:episodic ataxia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:episodic ataxia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:erb's muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:erb's muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:escobar syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:escobar syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ethnologic --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ethnologic | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:etiology aspects --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:etiology aspects | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:evans syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:evans syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:exfoliation syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:exfoliation syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:exposure as collected domain --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:exposure as collected domain | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:eye diseases, hereditary --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:eye diseases, hereditary | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:factor v and factor viii, combined deficiency of --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:factor v and factor viii, combined deficiency of | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:familial atypical hemolytic uremic syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:familial atypical hemolytic uremic syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:familial c3b inhibitor deficiency syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:familial creutzfeldt-jakob --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:familial creutzfeldt-jakob | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:familial hemiplegic migraine --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:familial hemiplegic migraine | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:familial hypoaldosteronism --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:familial hypoaldosteronism | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:familial juvenile nephronophthisis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:familial juvenile nephronophthisis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:feingold syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:feingold syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:felty syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:felty syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:fetal alcohol syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:fetal alcohol syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:fetal methotrexate syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:fetal methotrexate syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:fetal retinoid syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:fetal retinoid syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:fetal warfarin syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:fetal warfarin syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:floating-harbor syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:floating-harbor syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:folinic acid responsive seizure syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:folinic acid responsive seizure syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:fraser syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:fraser syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:frasier syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:frasier syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:fronto-facio-nasal dysplasia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:fronto-facio-nasal dysplasia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:fused hemispheres (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:fused hemispheres (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:game friedman paradice syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:game friedman paradice syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:gardner syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:gardner syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:genetic disorder --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:genetic disorder | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:geniospasm 1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:geniospasm 1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:geroderma osteodysplastica --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:geroderma osteodysplastica | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:gerstmann-straussler-scheinker disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:gerstmann-straussler-scheinker disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:glaucoma --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:glaucoma | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:glucose transporter protein type 1 deficiency syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:glucose transporter protein type 1 deficiency syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:glutamate formiminotransferase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:glutamate formiminotransferase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:glutamate-cysteine ligase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:glutamate-cysteine ligase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:glutathione synthetase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:glutathione synthetase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type i --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:glycogen storage disease type i | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type iib --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:glycogen storage disease type iib | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type x --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:glycogen storage disease type x | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:griscelli syndrome type 2 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:griscelli syndrome type 2 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:gurrieri sammito bellussi syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:gurrieri sammito bellussi syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:gyrate atrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:gyrate atrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hard skin syndrome parana type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hard skin syndrome parana type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hecht syndrome (disorder) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hecht syndrome (disorder) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hemophagocytic syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hemophagocytic syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hepatolenticular degeneration --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hepatolenticular degeneration | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hepatorenal syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hepatorenal syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary benign intraepithelial dyskeratosis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary benign intraepithelial dyskeratosis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary coproporphyria --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary coproporphyria | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary corneal dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary corneal dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary factor x deficiency disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary factor x deficiency disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary factor xi deficiency disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary factor xi deficiency disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary factor xii deficiency disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary factor xii deficiency disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary fructose intolerance --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary fructose intolerance | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary oculoleptomeningeal amyloid angiopathy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hereditary optic atrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hereditary optic atrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hermansky-pudlak syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hermansky-pudlak syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:heterotaxy syndrome with asplenia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:heterotaxy syndrome with asplenia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:heterotaxy syndrome with polysplenia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:heterotaxy syndrome with polysplenia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:histidinemia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:histidinemia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hnsha due to aldolase a deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hnsha due to aldolase a deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hnsha due to glutathione reductase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hnsha due to glutathione reductase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hnsha due to glutathione synthetase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hnsha due to glutathione synthetase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hnsha due to pyrimidine-5'-nucleotidase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:holmes-adie syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:holmes-adie syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:holoprosencephaly with fetal akinesia-hypokinesia sequence --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hunter syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hunter syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hydrocephalus with cerebellar agenesis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hydrocephalus with cerebellar agenesis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hypermanganesemia with dystonia polycythemia and cirrhosis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hypermanganesemia with dystonia polycythemia and cirrhosis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hyperplastic primary vitreous (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hyperplastic primary vitreous (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hyperprolinemia type 2 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hyperprolinemia type 2 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hyperviscosity syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hyperviscosity syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hypokalemia, familial --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hypokalemia, familial | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hypoplasia of the brainstem --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hypoplasia of the brainstem | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hypoplastic left heart syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hypoplastic left heart syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hypoplastic right heart syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hypoplastic right heart syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:hypospadias-mental retardation syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:hypospadias-mental retardation syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:immune reconstitution inflammatory syndrome associated with kaposi sarcoma | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:immunodeficiency syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:immunodeficiency syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:immunology aspects --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:immunology aspects | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:in cerebrospinal fluid --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:in cerebrospinal fluid | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:infantile hypophosphatasia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:infantile hypophosphatasia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:insulin autoimmune syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:insulin autoimmune syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:iris malformation or hypoplasia (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:iris malformation or hypoplasia (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:isaacs syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:isaacs syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:isolated hypoplasia of the right ventricle --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:isolated hypoplasia of the right ventricle | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:jackson-weiss syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:jackson-weiss syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:jeune syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:jeune syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kabuki syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kabuki syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kallmann syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kallmann syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kartagener syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kartagener syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kaufman-mckusick syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kaufman-mckusick syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kawasaki disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kawasaki disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kbg syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kbg syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kearns-sayre syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kearns-sayre syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:klinefelter syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:klinefelter syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kluver-bucy syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kluver-bucy syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:knuckle pads, leuconychia and sensorineural deafness --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:knuckle pads, leuconychia and sensorineural deafness | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kohlschutter tonz syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kohlschutter tonz syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:korsakoff syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:korsakoff syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:kshv inflammatory cytokine syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:kshv inflammatory cytokine syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:landau-kleffner syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:landau-kleffner syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:late-onset muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:late-onset muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:lateral medullary syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:lateral medullary syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:laurence-moon syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:laurence-moon syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:leber congenital amaurosis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:leber congenital amaurosis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:leigh disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:leigh disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:lesch-nyhan syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:lesch-nyhan syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:leukodystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:leukodystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:leukotriene c4 synthase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:leukotriene c4 synthase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:liddle syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:liddle syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:lig4 syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:lig4 syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:limb-girdle muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:limb-girdle muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:lipoid proteinosis of urbach and wiethe | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:lissencephaly, x-linked, 2 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:lissencephaly, x-linked, 2 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:long qt syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:long qt syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:lupus anticoagulant disorder --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:lupus anticoagulant disorder | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:lymphedema-distichiasis syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:lymphedema-distichiasis syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:macdermot winter syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:macdermot winter syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:majority of wws patients die within the first year of life --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:majority of wws patients die within the first year of life | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:mallory-weiss syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:mallory-weiss syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:marfan syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:marfan syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:marles greenberg persaud syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:marles greenberg persaud syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:maroteaux-lamy syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:maroteaux-lamy syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:marshall syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:marshall syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:masa syndrome (disorder) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:masa syndrome (disorder) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:meckel-gruber syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:meckel-gruber syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:meconium plug syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:meconium plug syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:melas syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:melas syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:melnick-fraser syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:melnick-fraser syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:meningoencephalocele (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:meningoencephalocele (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:menopausal muscular dystrophy syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:menopausal muscular dystrophy syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:menopausal syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:menopausal syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:mental retardation, profound (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:mental retardation, profound (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:merosin-deficient congenital muscular dystrophy type 1a --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:merosin-deficient congenital muscular dystrophy type 1a | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:merrf syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:merrf syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:microcephaly --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:microcephaly | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:microcephaly deafness syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:microcephaly deafness syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:microcephaly microcornea syndrome seemanova type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:microcephaly microcornea syndrome seemanova type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:miller-dieker syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:miller-dieker syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:miyoshi muscular dystrophy 1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:miyoshi muscular dystrophy 1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:mmih syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:mmih syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:mobius syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:mobius syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:moloney syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:moloney syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:monosomy 13q syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:monosomy 13q syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:morm syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:morm syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:multiple organ failure --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:multiple organ failure | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:multiple system malformation syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:multiple system malformation syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscle amp deaminase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscle amp deaminase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscle biopsy shows decreased glycosylation of alpha-dystroglycan (dag1, 128239) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscle biopsy shows decreased glycosylation of alpha-dystroglycan (dag1, 128239) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscle-eye-brain disease, congenital muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscle-eye-brain disease, congenital muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophies and other myopathies --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophies and other myopathies | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophy, congenital, with central nervous system involvement --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophy, congenital, with central nervous system involvement | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophy, limb-girdle, type 2k --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophy, limb-girdle, type 2k | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophy, oculopharyngeal --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophy, oculopharyngeal | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophy, scapulohumeral --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophy, scapulohumeral | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophy-deafmutism syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophy-deafmutism syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 6 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 6 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:muscular dystrophy-dystroglycanopathy (limb-girdle) type c, 5 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:muscular dystrophy-dystroglycanopathy (limb-girdle) type c, 5 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:myopathy with exercise intolerance, swedish type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:myopathy with exercise intolerance, swedish type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:myopia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:myopia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:myotonic dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:myotonic dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:nance-horan syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:nance-horan syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:naxos disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:naxos disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:neonatal research network terminology --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:neonatal research network terminology | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:neoplastic syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:neoplastic syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:nephrotic syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:nephrotic syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:netherton syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:netherton syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:neu-laxova syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:neu-laxova syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:neuraminidase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:neuraminidase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:neuroleptic malignant syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:neuroleptic malignant syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:neutral lipid storage disease with myopathy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:neutral lipid storage disease with myopathy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:niemann-pick disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:niemann-pick disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:non-polyposis turcot syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:non-polyposis turcot syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:nursing therapy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:nursing therapy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:obstructive sleep apnea syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:obstructive sleep apnea syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:oculo-palato-digital syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:oculo-palato-digital syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:oculo-respiratory syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:oculo-respiratory syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:oculocerebrorenal syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:oculocerebrorenal syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:oculocutaneous albinism type 4 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:oculocutaneous albinism type 4 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:oculodento-osseous dysplasia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:oculodento-osseous dysplasia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:oculomandibular dysostosis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:oculomandibular dysostosis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:oculorespiratory syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:oculorespiratory syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:onset prenatally or at birth --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:onset prenatally or at birth | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:optic nerve hypoplasia (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:optic nerve hypoplasia (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:organic brain syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:organic brain syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:orofaciodigital syndrome type 1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:orofaciodigital syndrome type 1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:orotic aciduria --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:orotic aciduria | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:otoonychoperoneal syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:otoonychoperoneal syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:otopalatodigital syndrome type 1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:otopalatodigital syndrome type 1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:overgrowth syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:overgrowth syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:overlap syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:overlap syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pachydermoperiostosis - familial --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pachydermoperiostosis - familial | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pachygyria with preferential frontoparietal involvement (meb) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pachygyria with preferential frontoparietal involvement (meb) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pallister-hall syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pallister-hall syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pallister-killian syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pallister-killian syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:palmar-plantar erythodysthesia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:palmar-plantar erythodysthesia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:papillon-lefevre syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:papillon-lefevre syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:paraneoplastic syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:paraneoplastic syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:parasitology --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:parasitology | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:paroxysmal extreme pain disorder --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:paroxysmal extreme pain disorder | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pathological aspects --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pathological aspects | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:patients with meb may acquire ability to walk and a few words --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:patients with meb may acquire ability to walk and a few words | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pearson marrow-pancreas syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pearson marrow-pancreas syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:peeling skin syndrome, acral type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:peeling skin syndrome, acral type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pelizaeus merzbacher like disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pelizaeus merzbacher like disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pena-shokeir syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pena-shokeir syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:penta x syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:penta x syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:perlman syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:perlman syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:peutz-jeghers syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:peutz-jeghers syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pharmacotherapeutic --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pharmacotherapeutic | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:piriformis muscle syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:piriformis muscle syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pituitary adenoma, familial isolated (disorder) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pituitary adenoma, familial isolated (disorder) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:poems syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:poems syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:poland syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:poland syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:polymicrogyria (meb) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:polymicrogyria (meb) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:polymyalgia rheumatica --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:polymyalgia rheumatica | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pomt1, 1-bp ins, 2110g --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pomt1, 1-bp ins, 2110g | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pomt1, 2-bp del, 2179tc --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pomt1, 2-bp del, 2179tc | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pomt1, 3-bp del, 1260cct --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pomt1, 3-bp del, 1260cct | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pomt1, gly76arg --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pomt1, gly76arg | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:popliteal pterygium syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:popliteal pterygium syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:posterior fossa syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:posterior fossa syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:potocki-lupski syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:potocki-lupski syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:presentey anomaly --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:presentey anomaly | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:primary fanconi syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:primary fanconi syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:primary hyperoxaluria --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:primary hyperoxaluria | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:progeria --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:progeria | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:progressive familial intrahepatic cholestasis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:progressive familial intrahepatic cholestasis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:progressive hemifacial atrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:progressive hemifacial atrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:progressive supranuclear palsy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:progressive supranuclear palsy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:prolonged electroretinal response suppression --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:prolonged electroretinal response suppression | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:proteus syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:proteus syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:prune belly syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:prune belly syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:psychology qualifier --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:psychology qualifier | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pulmonic stenosis and congenital nephrosis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pulmonic stenosis and congenital nephrosis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pyle metaphyseal dysplasia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pyle metaphyseal dysplasia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pyramidal tract dysfunction --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pyramidal tract dysfunction | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:pyruvate carboxylase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:pyruvate carboxylase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:radial aplasia-thrombocytopenia syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:radial aplasia-thrombocytopenia syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:radiotherapeutic --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:radiotherapeutic | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:rapadilino syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:rapadilino syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:renal cysts and diabetes syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:renal cysts and diabetes syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:renal dysplasia (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:renal dysplasia (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:retinal dysplasia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:retinal dysplasia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:retinal malformations (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:retinal malformations (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:retinitis punctata albescens (disorder) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:retinitis punctata albescens (disorder) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:rett syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:rett syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:richards-rundle syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:richards-rundle syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:rieger syndrome type 1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:rieger syndrome type 1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:rna polymerase iii-related leukodystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:rna polymerase iii-related leukodystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:roentgenographic --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:roentgenographic | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:rud syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:rud syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:sandifer's syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:sandifer's syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:sarcosinemia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:sarcosinemia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:schinzel-giedion midface-retraction syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:schinzel-giedion midface-retraction syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:scimitar syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:scimitar syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:sellars beighton syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:sellars beighton syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:severe childhood autosomal recessive muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:severe childhood autosomal recessive muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:severe disorder --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:severe disorder | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:severe early childhood onset retinal dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:severe early childhood onset retinal dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:severe muscular hypotonia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:severe muscular hypotonia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:severe steroid 21-hydroxylase deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:shprintzen-goldberg craniosynostosis syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:shprintzen-goldberg craniosynostosis syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:shwachman-diamond syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:shwachman-diamond syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:simpson golabi behmel syndrome type 1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:simpson golabi behmel syndrome type 1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:sjogren syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:sjogren syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:sjogren-larsson syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:sjogren-larsson syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:sly syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:sly syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:smith-lemli-opitz syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:smith-lemli-opitz syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:smith-magenis syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:smith-magenis syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:smith-mccort dysplasia --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:smith-mccort dysplasia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:soft tissue --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:soft tissue | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:solitary median maxillary central incisor --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:solitary median maxillary central incisor | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:somnolence syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:somnolence syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:sonoda syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:sonoda syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:spastic paraplegia 15, autosomal recessive --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:spastic paraplegia 15, autosomal recessive | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:spondylo-ocular syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:spondylo-ocular syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:spondylocarpotarsal synostosis syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:staphylococcal scalded skin syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:staphylococcal scalded skin syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:stevens-johnson syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:stevens-johnson syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:stickler syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:stickler syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:stiff person syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:stiff person syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:substance withdrawal syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:substance withdrawal syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:tarsal tunnel syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:tarsal tunnel syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:taxonomic --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:taxonomic | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:tay-sachs disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:tay-sachs disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:teething syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:teething syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:thalidomide embryopathy syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:thalidomide embryopathy syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:thyroid dyshormonogenesis 4 --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:thyroid dyshormonogenesis 4 | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:tooth and nail syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:tooth and nail syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:tourette syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:tourette syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:transcobalamin ii deficiency --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:transcobalamin ii deficiency | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:trichohepatoenteric syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:trichohepatoenteric syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:trichorhinophalangeal syndrome type ii --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:trichorhinophalangeal syndrome type ii | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:trichothiodystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:trichothiodystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:tubulointerstitial nephritis and uveitis --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:tubulointerstitial nephritis and uveitis | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:tyrosinemia, type iii --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:tyrosinemia, type iii | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:ullrich congenital muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ullrich congenital muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:uveitis glaucoma and hyphema syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:uveitis glaucoma and hyphema syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:uveomeningoencephalitic syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:uveomeningoencephalitic syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:van der woude syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:van der woude syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:verloes bourguignon syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:verloes bourguignon syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:vertebral artery syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:vertebral artery syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:veterinary aspects --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:veterinary aspects | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:virtually no active movement at birth (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:virtually no active movement at birth (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:vitreoretinal dysgenesis (wws) --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:vitreoretinal dysgenesis (wws) | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:von hippel-lindau syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:von hippel-lindau syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:waardenburg syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:waardenburg syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:waisman syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:waisman syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:walker-warburg congenital muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:walker-warburg congenital muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:walker-warburg syndrome, fktn-related --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:walker-warburg syndrome, fktn-related | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:warsaw breakage syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:warsaw breakage syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:waterhouse-friderichsen syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:waterhouse-friderichsen syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:weaver syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:weaver syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:werner syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:werner syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:west syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:west syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:white matter changes --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:white matter changes | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:wiskott-aldrich syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:wiskott-aldrich syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:wolf-hirschhorn syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:wolf-hirschhorn syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:wolff-parkinson-white syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:wolff-parkinson-white syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:wolman disease --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:wolman disease | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:woodhouse sakati syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:woodhouse sakati syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:x-linked emery-dreifuss muscular dystrophy --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:x-linked emery-dreifuss muscular dystrophy | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:x-linked lissencephaly --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:x-linked lissencephaly | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:xanthinuria, type i --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:xanthinuria, type i | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:xxyy syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:xxyy syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:xyy syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:xyy syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 en:yellow nail syndrome --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:yellow nail syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 hydrocéphalie --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=hydrocéphalie | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 hypogonadisme avec anosmie --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=hypogonadisme avec anosmie | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 oeil --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=oeil | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 processus pathologique --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=processus pathologique | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 protein O-mannosyl-transferases --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=protein O-mannosyl-transferases | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 syndrome de Chemke --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Chemke | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 syndrome de warburg --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de warburg | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 œil --- r_associated #0: 20 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=œil | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20 Kallman --- r_associated #0: 15 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=Kallman | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=15 Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=Syndrome de Walker-Warburg | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=15 syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Kallman-de Morsier | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=15 syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de de Morsier-Kallmann | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=15 albinisme --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=albinisme | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 association de tics vocaux et tics moteurs du syndrome de gilles de la tourette --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=association de tics vocaux et tics moteurs du syndrome de gilles de la tourette | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 dumping syndrome --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=dumping syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 dystrophie musculaire --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=dystrophie musculaire | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 dystrophie myotonique --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=dystrophie myotonique | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 défaillance multi-viscérale --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=défaillance multi-viscérale | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 défaillance multiviscérale --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=défaillance multiviscérale | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 déficit en cytochrome oxydase --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=déficit en cytochrome oxydase | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 en:eds --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:eds | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 en:ehlers danlos syndrome --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ehlers danlos syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 glaucome capsulaire --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=glaucome capsulaire | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 hypophosphatasie foetale --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=hypophosphatasie foetale | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 hypophosphatasie infantile --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=hypophosphatasie infantile | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 maladie de Gilles de la Tourette --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=maladie de Gilles de la Tourette | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 maladie des tics --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=maladie des tics | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 maladie des tics de Gilles de la Tourette --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=maladie des tics de Gilles de la Tourette | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 maladies de gilles de la tourette --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=maladies de gilles de la tourette | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 polymyalgia rheumatica --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=polymyalgia rheumatica | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 progeria --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=progeria | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome adéno-cutanéo-muqueux --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome adéno-cutanéo-muqueux | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome de Gilles de la Tourette --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Gilles de la Tourette | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome de Rett --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Rett | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome de Warburg --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Warburg | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome de de Morsier --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de de Morsier | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome de défaillance multiviscérale --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de défaillance multiviscérale | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome de la Tourette --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de la Tourette | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome de la selle turcique vide --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de la selle turcique vide | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome de tourette --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de tourette | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome des tics de Gilles de la Tourette --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome des tics de Gilles de la Tourette | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome malin d'un neuroleptique --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome malin d'un neuroleptique | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome malin de neuroleptiques --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome malin de neuroleptiques | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 syndrome malin des neuroleptiques --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome malin des neuroleptiques | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 trouble de gilles de la tourette --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=trouble de gilles de la tourette | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 ventriculomégalie cérébrale --- r_associated #0: 10 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=ventriculomégalie cérébrale | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=10 dystrophie musculaire oculo-pharyngée --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=dystrophie musculaire oculo-pharyngée | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 dystrophie musculaire oculopharyngée --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=dystrophie musculaire oculopharyngée | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 défaillance polyviscérale --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=défaillance polyviscérale | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 en:Neuroleptic malignant syndrome --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:Neuroleptic malignant syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 en:cerebral ventriculomegaly --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:cerebral ventriculomegaly | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 en:ventriculomeglia --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=en:ventriculomeglia | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 hyperoxalurie primitive --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=hyperoxalurie primitive | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 maladie de Kawasaki --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=maladie de Kawasaki | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 maladie de Wolman --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=maladie de Wolman | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 myopathie primitive progressive --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=myopathie primitive progressive | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 snm --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=snm | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 syndrome adénocutanéomuqueux --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome adénocutanéomuqueux | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 syndrome d'Ehlers-Danlos --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome d'Ehlers-Danlos | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 syndrome de Duane --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Duane | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 syndrome de Kawasaki --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Kawasaki | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 syndrome de Stickler --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Stickler | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 syndrome de Türk-Stilling-Duane --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Türk-Stilling-Duane | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 syndrome de Wolff-Parkinson-White --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome de Wolff-Parkinson-White | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 syndrome malin neuroleptique --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome malin neuroleptique | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5 syndrome olfacto-génital --- r_associated #0: 5 --> en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) n1=syndrome olfacto-génital | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=5