'en:crouzon syndrome with acanthosis nigricans (disorder)'
(id=6819745 ; fe=en:crouzon syndrome with acanthosis nigricans (disorder) ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=28418 creation date=2017-06-25 touchdate=2025-08-21 12:08:25.000)

≈ 637 relations sortantes en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 43 / 1 -> en:alpha-fetoprotein, hereditary persistence of n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:alpha-fetoprotein, hereditary persistence of | rel=r_associated | relid=0 | w=43 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 43 / 1 -> en:dyskeratosis congenita n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dyskeratosis congenita | rel=r_associated | relid=0 | w=43 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 43 / 1 -> en:fibrodysplasia ossificans progressiva n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=43 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 43 / 1 -> en:klippel-trenaunay-weber syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:klippel-trenaunay-weber syndrome | rel=r_associated | relid=0 | w=43 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 43 / 1 -> en:sebastian syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:sebastian syndrome | rel=r_associated | relid=0 | w=43 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 42 / 0.977 -> en:insulin autoimmune syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:insulin autoimmune syndrome | rel=r_associated | relid=0 | w=42 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 42 / 0.977 -> en:macular corneal dystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=42 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 42 / 0.977 -> en:marfan syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=42 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 42 / 0.977 -> en:multiple self healing epithelioma of ferguson-smith n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:multiple self healing epithelioma of ferguson-smith | rel=r_associated | relid=0 | w=42 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 41 / 0.953 -> en:hereditary palmoplantar keratoderma gamborg nielsen type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=41 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 41 / 0.953 -> en:inherited arthrogryposis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:inherited arthrogryposis | rel=r_associated | relid=0 | w=41 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 41 / 0.953 -> en:spinocerebellar ataxia 28 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia 28 | rel=r_associated | relid=0 | w=41 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 41 / 0.953 -> en:wnt4 mullerian aplasia and ovarian dysfunction n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:wnt4 mullerian aplasia and ovarian dysfunction | rel=r_associated | relid=0 | w=41 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 40 / 0.93 -> en:cochleosaccular degeneration of the inner ear and progressive cataracts n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=40 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 40 / 0.93 -> en:genitopatellar syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:genitopatellar syndrome | rel=r_associated | relid=0 | w=40 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 40 / 0.93 -> en:hereditary gastrogenic lactose intolerance n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary gastrogenic lactose intolerance | rel=r_associated | relid=0 | w=40 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 40 / 0.93 -> en:hyperinsulinism due to deficiency of glucokinase n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperinsulinism due to deficiency of glucokinase | rel=r_associated | relid=0 | w=40 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 39 / 0.907 -> en:hereditary mucosal leukokeratosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=39 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 38 / 0.884 -> en:epiphyseal dysplasia, multiple, 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:epiphyseal dysplasia, multiple, 1 | rel=r_associated | relid=0 | w=38 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 38 / 0.884 -> en:nevoid basal cell carcinoma syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:nevoid basal cell carcinoma syndrome | rel=r_associated | relid=0 | w=38 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 38 / 0.884 -> en:spondylo-ocular syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=38 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 37 / 0.86 -> en:cleft lip/palate-ectodermal dysplasia syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=37 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 37 / 0.86 -> en:congenital abnormality n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=37 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 36 / 0.837 -> en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | rel=r_associated | relid=0 | w=36 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:acute intermittent porphyria n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:antley-bixler syndrome, autosomal dominant n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:autosomal dominant charcot-marie-tooth disease type 2a1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant charcot-marie-tooth disease type 2a1 | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:autosomal dominant hypophosphatemic bone disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant hypophosphatemic bone disease | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:autosomal dominant optic atrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:baller-gerold syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:centronuclear myopathy 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:centronuclear myopathy 1 | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:cerebellar ataxia ectodermal dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:chronic infantile neurological cutaneous and articular syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:chronic infantile neurological cutaneous and articular syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:cleidocranial dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:congenital bowing of long bone n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:congenital nephrogenic diabetes insipidus n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:cystinosis, infantile nephropathic n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cystinosis, infantile nephropathic | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:epidermolysis bullosa simplex with pyloric atresia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:epilepsy, myoclonic, benign adult familial, type 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:familial amyloid neuropathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial amyloid neuropathy | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:fronto-facio-nasal dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:gaze palsy, familial horizontal, with progressive scoliosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:goniodysgenesis-mental retardation-short stature syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:heide syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:heide syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:hereditary benign intraepithelial dyskeratosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:hereditary hemorrhagic telangiectasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary hemorrhagic telangiectasia | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:hypermobility syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypermobility syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:jackson-weiss syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:keratosis palmoplantaris papulosa n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:keratosis palmoplantaris papulosa | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:liddle syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:may-hegglin anomaly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:may-hegglin anomaly | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:metaphyseal dysplasia, braun-tinschert type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:metaphyseal dysplasia, braun-tinschert type | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:microcephaly cervical spine fusion anomalies n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:microcephaly deafness syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:mowat-wilson syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:myopathy with abnormal lipid metabolism n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:myopathy with abnormal lipid metabolism | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:naxos disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:naxos disease | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:nonaka myopathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:oculocutaneous albinism n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:oculocutaneous albinism | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:osteogenesis imperfecta, levin type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:osteogenesis imperfecta, levin type | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:palmoplantar porokeratosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:palmoplantar porokeratosis | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:pseudocholinesterase deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:roch leri mesosomatous lipomatosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:roch leri mesosomatous lipomatosis | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:rothmund-thomson syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:rothmund-thomson syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:schnyder crystalline corneal dystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:schnyder crystalline corneal dystrophy | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 36 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia 36 | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia type 4 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia type 4 | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:spondylocamptodactyly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondylocamptodactyly | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:steinfeld syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:syndromic orbital border hypoplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:type ii acrocephalopolysyndactyly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 35 / 0.814 -> en:vitelliform macular dystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:autosomal dominant progressive nephropathy with hypertension n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant progressive nephropathy with hypertension | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:autosomal recessive muscular dystrophy with limb girdle distribution n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:bannayan syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:bannayan syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:brachydactyly syndrome type b n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:capillary malformation-arteriovenous malformation (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:capillary malformation-arteriovenous malformation (disorder) | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:cutis laxa, autosomal dominant n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cutis laxa, autosomal dominant | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:dominant autosomal hereditary disorder, incomplete penetrance n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dominant autosomal hereditary disorder, incomplete penetrance | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:dopa-responsive dystonia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:ehlers-danlos syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:familial acantholysis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:familial amyloid polyneuropathy, type v n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial amyloid polyneuropathy, type v | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:familial benign neonatal epilepsy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:familial osteochondritis dissecans n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial osteochondritis dissecans | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:femur bifid with monodactylous ectrodactyly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:femur bifid with monodactylous ectrodactyly | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:freeman-sheldon syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:generalized myotonia of thomsen n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:generalized myotonia of thomsen | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:giacci familial neurogenic acroosteolysis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:glomuvenous malformations n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:glomuvenous malformations | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:hereditary elliptocytosis due to abnormal protein 4.1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary elliptocytosis due to abnormal protein 4.1 | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:hereditary elliptocytosis due to alpha spectrin defect n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary elliptocytosis due to alpha spectrin defect | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:hereditary oculoleptomeningeal amyloid angiopathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:hereditary tubulointerstitial disorder n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary tubulointerstitial disorder | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:hyperinsulinemic hypoglycemia, familial, 7 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperinsulinemic hypoglycemia, familial, 7 | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:hypotrichosis simplex of scalp n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypotrichosis simplex of scalp | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:kbg syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:knobloch syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:lynch syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:lynch syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:mandibuloacral dysplasia with type a lipodystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:multiple epiphyseal dysplasia type 5 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:multiple epiphyseal dysplasia type 5 | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:myopathy, distal 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:myopathy, distal 2 | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:neurofibromatosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:neurofibromatosis | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:neurofibromatosis type 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:neurofibromatosis type 1 | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:parietal foramina n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:parietal foramina | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:partington x-linked mental retardation syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:partington x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:piebaldism n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:piebaldism | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:polydactyly, preaxial ii (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:rhizomelic chondrodysplasia punctata n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:rhizomelic chondrodysplasia punctata | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:short stature with valvular heart disease and characteristic facies syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:short stature with valvular heart disease and characteristic facies syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 29 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia 29 | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia type 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia type 2 | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:spondylocostal dysostosis 4, autosomal dominant n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:steatocystoma multiplex n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:steatocystoma multiplex | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:tarsal-carpal coalition syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:uv-sensitive syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:wellesley carman french syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 34 / 0.791 -> en:wells jankovic syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:wells jankovic syndrome | rel=r_associated | relid=0 | w=34 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:acrodermatitis enteropathica n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:acromicric dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:advanced sleep-phase syndrome, familial n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:advanced sleep-phase syndrome, familial | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:aplasia of lacrimal and salivary glands n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:arthrogryposis, distal, type 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:arthrogryposis, distal, type 1 | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:atelosteogenesis, type 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:atelosteogenesis, type 1 | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:autosomal dominant charcot-marie-tooth disease type 2c n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant charcot-marie-tooth disease type 2c | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:autosomal dominant epidermolysis bullosa simplex n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:autosomal recessive distal osteolysis syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:benign autosomal dominant osteopetrosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:benign autosomal dominant osteopetrosis | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:brachyolmia type 3 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:choreoathetosis/spasticity, episodic n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:chromosome 3q29 deletion syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:chromosome 3q29 deletion syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:cole disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cole disease | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:currarino triad n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:currarino triad | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:disseminated superficial porokeratosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:disseminated superficial porokeratosis | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:ectodermal dysplasia/ skin fragility syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:familial encephalopathy with neuroserpin inclusion bodies n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:familial hypodontia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial hypodontia | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:fleck corneal dystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:fleck corneal dystrophy | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:haspeslagh fryns muelenaere syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:hereditary diffuse gastric adenocarcinoma n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary diffuse gastric adenocarcinoma | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:hereditary motor and sensory neuropathy type i n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary motor and sensory neuropathy type i | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:hyperpigmentation, familial progressive n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperpigmentation, familial progressive | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:hypoplastic tibia and postaxial polydactyly syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:iris coloboma with ptosis, hypertelorism, and mental retardation n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:iris coloboma with ptosis, hypertelorism, and mental retardation | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:klippel-feil syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:klippel-feil syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:laurin-sandrow syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:lissencephaly syndrome, norman-roberts type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:macdermot winter syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:muckle-wells syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:muckle-wells syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:multicentric osteolysis nodulosis arthropathy spectrum n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:neuropathy, hereditary thermosensitive n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:neuropathy, hereditary thermosensitive | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:peripheral resistance to thyroid hormone n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:peripheral resistance to thyroid hormone | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:peutz-jeghers syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:pili torti-deafness syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pili torti-deafness syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:radial hypoplasia, triphalangeal thumbs and hypospadias n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:radial hypoplasia, triphalangeal thumbs and hypospadias | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:reardon hall slaney syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:reis-bucklers' corneal dystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:reis-bucklers' corneal dystrophy | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:robinow syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia type 5 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia type 5 | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:spondyloepiphyseal dysplasia tarda, toledo type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 32 / 0.744 -> en:strudwick syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:strudwick syndrome | rel=r_associated | relid=0 | w=32 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:acanthosis nigricans n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:acanthosis nigricans | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:andersen syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:auriculo-condylar syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:auriculo-condylar syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:autoimmune lymphoproliferative syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autoimmune lymphoproliferative syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:autosomal dominant polycystic kidney disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant polycystic kidney disease | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:cerebrotendinous xanthomatosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:charcot-marie-tooth disease type 2d n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:charcot-marie-tooth disease type 2d | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:charcot-marie-tooth disease, axonal, type 2e (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:charcot-marie-tooth disease, axonal, type 2l (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:chondrodysplasia punctata syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:congenital craniofacial dysostosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital craniofacial dysostosis | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:craniodiaphyseal dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:craniofacial deafness hand syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:craniofacial deafness hand syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:dyskeratosis congenita, autosomal dominant n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dyskeratosis congenita, autosomal dominant | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:dysplasia, saddan n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dysplasia, saddan | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:ehlers-danlos syndrome, type i n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ehlers-danlos syndrome, type i | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:familial arthrogryposis-cholestatic hepatorenal syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial arthrogryposis-cholestatic hepatorenal syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:familial cold autoinflammatory syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial cold autoinflammatory syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:familial isolated arrhythmogenic right ventricular dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial isolated arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:glycogen storage disease 0, liver n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:glycogen storage disease 0, liver | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:glycogen storage disease type x n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:gurrieri sammito bellussi syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:hand foot uterus syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hand foot uterus syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:hereditary sensory autonomic neuropathy, type 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary sensory autonomic neuropathy, type 1 | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:hereditary systemic amyloidosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary systemic amyloidosis | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:hnsha due to triosephosphate isomerase deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hnsha due to triosephosphate isomerase deficiency | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:hyperinsulinism due to hnf4a deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperinsulinism due to hnf4a deficiency | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:marden-walker syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:marden-walker syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:melanoma astrocytoma syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:nemaline myopathy 3 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:nemaline myopathy 3 | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:neurofibromatosis, type 1-like syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:neurofibromatosis, type 1-like syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:neuropathy, hereditary motor and sensory, okinawa type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:neuropathy, hereditary motor and sensory, okinawa type | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:oculocerebral hypopigmentation syndrome type preus n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:paroxysmal extreme pain disorder n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:peeling skin syndrome, acral type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:pituitary adenoma, familial isolated (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:pulmonary interstitial glycogenosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pulmonary interstitial glycogenosis | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:smith-mccort dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:split-hand-foot malformation with long bone deficiency 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:split-hand-foot malformation with long bone deficiency 1 | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:stickler syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:stickler syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:synpolydactyly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:thiel-behnke corneal dystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:thiel-behnke corneal dystrophy | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 31 / 0.721 -> en:turcot syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:turcot syndrome | rel=r_associated | relid=0 | w=31 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:angioma hereditary neurocutaneous n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:angioma hereditary neurocutaneous | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:autosomal dominant hyperinsulinism due to sur1 deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant hyperinsulinism due to sur1 deficiency | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:autosomal dominant pterygium of conjunctiva n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:bilateral multiple fibroadenoma of breast n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:bilateral multiple fibroadenoma of breast | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:bilateral pheochromocytoma and islet cell adenoma of the pancreas n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:cap myopathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cap myopathy | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:cerebral cavernous malformation n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:chromosome 22q11.2 microduplication syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:chromosome 22q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:dentatorubral-pallidoluysian atrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:dominant autosomal hereditary disorder, complete penetrance n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dominant autosomal hereditary disorder, complete penetrance | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:familial creutzfeldt-jakob n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:familial digital arthropathy and brachydactyly syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial digital arthropathy and brachydactyly syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:fibular hypoplasia and complex brachydactyly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:follicular atrophoderma and basal cell epitheliomata n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:follicular atrophoderma and basal cell epitheliomata | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:hallermann syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hallermann syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:hereditary cystatin c amyloid angiopathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:hypertelorism n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypertelorism | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:keratoacanthoma familial n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:keratoacanthoma familial | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:lamellar ichthyosis, autosomal dominant form n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:lamellar ichthyosis, autosomal dominant form | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:melnick-fraser syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:menkes disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:menkes disease | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:miller-mckusick-malvaux-syndrome (3m syndrome) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:morquio syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:muscle amp deaminase deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:nicolaides baraitser syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:oculodental syndrome rutherfurd syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:perniola krajewska carnevale syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:perniola krajewska carnevale syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:poikiloderma, hereditary sclerosing n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:poikiloderma, hereditary sclerosing | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:potassium aggravated myotonia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:potassium aggravated myotonia | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:proteus-like syndrome (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:reticulate acropigmentation of kitamura n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:reticulate acropigmentation of kitamura | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:saito kuba tsuruta syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:sitosterolemia with xanthomatosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia 1s n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia 1s | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia type 7 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia type 7 | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:spondyloepiphyseal dysplasia tarda, x-linked n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondyloepiphyseal dysplasia tarda, x-linked | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:spondyloperipheral dysplasia short ulna n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondyloperipheral dysplasia short ulna | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 30 / 0.698 -> en:syndactyly, type i n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:syndactyly, type i | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:acquired acanthosis nigricans n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:acquired acanthosis nigricans | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:acrodysostosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:acrodysostosis | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:amelogenesis imperfecta, type ib n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:amelogenesis imperfecta, type ib | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:angiokeratoma corporis diffusum n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:angiokeratoma corporis diffusum | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:autosomal dominant hyperinsulinism due to kir6.2 deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:autosomal dominant ichthyosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant ichthyosis | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:autosomal dominant late onset basal ganglia degeneration n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant late onset basal ganglia degeneration | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:autosomal dominant variant form of albumin n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant variant form of albumin | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:avascular necrosis of femoral head n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:avascular necrosis of femoral head | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:becker generalized myotonia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:brachydactyly type a6 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:brachydactyly type a6 | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:brody myopathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:brody myopathy | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:cerebral hemorrhage with amyloidosis, hereditary, dutch type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:charcot-marie-tooth disease, type 2j n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:charcot-marie-tooth disease, type 2j | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:congenital premature fusion n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital premature fusion | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:corneal dystrophy, congenital stromal n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:corneal dystrophy, congenital stromal | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:dysostosis multiplex group n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dysostosis multiplex group | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:dystonia 12 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:ectodermal dysplasia with natal teeth, turnpenny type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ectodermal dysplasia with natal teeth, turnpenny type | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:familial spontaneous pneumothorax n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial spontaneous pneumothorax | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:feingold syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:geroderma osteodysplastica n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:hereditary cerebral amyloid angiopathy, icelandic type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:hereditary myopathy with early respiratory failure n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:heritable pulmonary arterial hypertension due to bmpr2 mutation n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:hyperferritinemia, hereditary, with congenital cataracts n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:kohlschutter tonz syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:kohlschutter tonz syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:leopard syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:lethal congenital contracture syndrome 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:li-fraumeni syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:loeys-dietz syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:microcornea with glaucoma and absent frontal sinus syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:myopathy with exercise intolerance, swedish type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:non-dystrophic myotonia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:non-dystrophic myotonia | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:papillon-lefevre syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:potocki-shaffer syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:pseudohypoaldosteronism, type 1, dominant form n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pseudohypoaldosteronism, type 1, dominant form | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:schinzel-giedion midface-retraction syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia 31 (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia 31 (disorder) | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia type 6 (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia type 6 (disorder) | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:spondyloenchondrodysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:sting-associated vasculopathy with onset in infancy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:sting-associated vasculopathy with onset in infancy | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:syndactyly, type iii n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:syndactyly, type iii | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:verloes bourguignon syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:vitreoretinochoroidopathy (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:vitreoretinochoroidopathy (disorder) | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 29 / 0.674 -> en:whyte hemingway carpal tarsal phalangeal osteolyses n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:whyte hemingway carpal tarsal phalangeal osteolyses | rel=r_associated | relid=0 | w=29 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> anomalie congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=anomalie congénitale | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:albinoidism n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:albinoidism | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:atrophoderma vermiculatum n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:autosomal dominant deficiency of plasminogen n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant deficiency of plasminogen | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:autosomal dominant familial woolly hair n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant familial woolly hair | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:autosomal dominant idiopathic familial dystonia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:autosomal dominant muscular dystrophy not predominantly limb girdle n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant muscular dystrophy not predominantly limb girdle | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:behavioral variant of frontotemporal dementia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:blau syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:blau syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:brachydactyly, type a1 (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:brachydactyly, type a1 (disorder) | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:cataract, congenital, cerulean type 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cataract, congenital, cerulean type 1 | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:char syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:char syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:col1a1 associated connective tissue disorder n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:col1a1 associated connective tissue disorder | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:congenital n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:congenital dyserythropoietic anemia, type iii n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital dyserythropoietic anemia, type iii | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:congenital ichthyosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital ichthyosis | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:crouzon syndrome with acanthosis nigricans, ala391glu (allelic variant) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:crouzon syndrome with acanthosis nigricans, ala391glu (allelic variant) | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:dicer1 syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dicer1 syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:dysplastic nevus syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dysplastic nevus syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:dystrophia myotonica 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dystrophia myotonica 2 | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:epithelial recurrent erosion dystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:epithelial recurrent erosion dystrophy | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:familial amyloid polyneuropathy with cutaneous amyloidosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial amyloid polyneuropathy with cutaneous amyloidosis | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:frontotemporal dementia, chromosome 3-linked n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:geniospasm 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:glycogen storage disease, muscular form n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:glycogen storage disease, muscular form | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:hereditary angioedema n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:hereditary nonpolyposis colorectal cancer n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary nonpolyposis colorectal cancer | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:hereditary papillary renal cell carcinoma n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary papillary renal cell carcinoma | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:hypophosphatemic rickets with hypercalciuria, hereditary n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:lethal congenital contracture syndrome type 3 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:lipoid proteinosis of urbach and wiethe n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:mullerian duct and limb anomalies syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:mullerian duct and limb anomalies syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:muscle l-lactate dehydrogenase deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:muscle l-lactate dehydrogenase deficiency | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:nail-patella syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:noonan syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:okihiro syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:prune belly syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:shwachman-diamond syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:shwachman-diamond syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia 10 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia 10 | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia 8 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia 8 | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:spondyloenchondrodysplasia with immune dysregulation n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:transthyretin related familial amyloid cardiomyopathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:transthyretin related familial amyloid cardiomyopathy | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:type i acrocephalosyndactyly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:type i acrocephalosyndactyly | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:type v acrocephalosyndactyly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:type v acrocephalosyndactyly | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 28 / 0.651 -> en:ulna metaphyseal dysplasia syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ulna metaphyseal dysplasia syndrome | rel=r_associated | relid=0 | w=28 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:acanthosis nigricans of oral mucous membranes n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:acanthosis nigricans of oral mucous membranes | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:adult onset autosomal dominant leukodystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:adult onset autosomal dominant leukodystrophy | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:ameloonychohypohidrotic syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ameloonychohypohidrotic syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:ataxia telangiectasia syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:autosomal dominant cystoid macular edema n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant cystoid macular edema | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:autosomal dominant retinitis pigmentosa n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant retinitis pigmentosa | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:benign congenital myopathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:benign congenital myopathy | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:charcot-marie-tooth disease, axonal, type 2b (disorder) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:congenital hereditary muscular dystrophy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital hereditary muscular dystrophy | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:craniofacial dysostosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:craniofacial dysostosis | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:cutis laxa, autosomal recessive n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:deafness-craniofacial syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:dentin dyspalsia, shields type 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dentin dyspalsia, shields type 2 | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:episodic ataxia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:familial hemiplegic migraine n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:familial hypercalciuric hypocalcemia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial hypercalciuric hypocalcemia | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:familial interstitial nephritis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial interstitial nephritis | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:farber lipogranulomatosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:glucose transporter protein type 1 deficiency syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:glucose transporter protein type 1 deficiency syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:hereditary breast and ovarian cancer syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary breast and ovarian cancer syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:hereditary elliptocytosis due to beta spectrin defect in self-association n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary elliptocytosis due to beta spectrin defect in self-association | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:hereditary stomatocytosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary stomatocytosis | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:hyaline dystrophy of bruch's membrane n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyaline dystrophy of bruch's membrane | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:hyperinsulinemic hypoglycemia, familial, 6 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperinsulinemic hypoglycemia, familial, 6 | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:majeed syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:mesomelic dwarfism reinhardt pfeiffer type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:mesomelic dwarfism reinhardt pfeiffer type | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:microphthalmia, syndromic 3 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:multiple endocrine neoplasia type 2b n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:multiple endocrine neoplasia type 2b | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:myopathy, distal, tateyama type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:myopathy, distal, tateyama type | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:ocular albinism-lentigines-deafness syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ocular albinism-lentigines-deafness syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:polyostotic fibrous dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:polyostotic fibrous dysplasia | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:popliteal pterygium syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:primary hypertrophic osteoarthropathy n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:primary hypertrophic osteoarthropathy | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:spondyloepiphyseal dysplasia, omani type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:treacher collins syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:tylosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:tylosis | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:ulnar-mammary syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ulnar-mammary syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> en:von willebrand disease, platelet type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:von willebrand disease, platelet type | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 27 / 0.628 -> syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome | rel=r_associated | relid=0 | w=27 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:alagille syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:autosomal dominant analbuminemia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant analbuminemia | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:autosomal dominant excess of transthyretin n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant excess of transthyretin | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:autosomal dominant ichthyosis vulgaris n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant ichthyosis vulgaris | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:autosomal dominant mutilating keratoderma n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant mutilating keratoderma | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:autosomal dominant oculocutaneous albinism n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant oculocutaneous albinism | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:beare-stevenson cutis gyrata syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:brachymesophalangy 2 and 5 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:brachymesophalangy 2 and 5 | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:brooke-spiegler syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:brooke-spiegler syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:chromosome 17q21.31 deletion syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:congenital reticular ichthyosiform erythroderma n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital reticular ichthyosiform erythroderma | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:distal arthrogryposis syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:distal arthrogryposis syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:dominant beta-thalassemia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dominant beta-thalassemia | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:familial non-autoimmune autosomal dominant hyperthyroidism n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial non-autoimmune autosomal dominant hyperthyroidism | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:familial partial lipodystrophy, type 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial partial lipodystrophy, type 2 | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:foxg1 syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:frontotemporal dementia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:generalized epilepsy and paroxysmal dyskinesia syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:hawkinsinuria n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hawkinsinuria | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:hereditary elliptocytosis due to deficiency of protein 4.1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary elliptocytosis due to deficiency of protein 4.1 | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:hereditary multiple exostoses n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:hyperparathyroidism-jaw tumor syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperparathyroidism-jaw tumor syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:keratitis, hereditary n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:keratitis, hereditary | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:kuskokwim disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:lethal congenital contracture syndrome 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:nathalie syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:neurofibromatosis type 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:neurofibromatosis type 2 | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:otoonychoperoneal syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:pitt-hopkins syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pitt-hopkins syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:premature aging syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:premature aging syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:pyle metaphyseal dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:radial aplasia-thrombocytopenia syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:radial aplasia-thrombocytopenia syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:sellars beighton syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:sellars beighton syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:shprintzen omphalocele syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:syndrome, branchio-oculo-facial n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:triglyceride storage disease with ichthyosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:triglyceride storage disease with ichthyosis | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:tuberous sclerosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:von hippel-lindau syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:von hippel-lindau syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:xeroderma pigmentosum n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 26 / 0.605 -> en:zimmerman laband syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:zimmerman laband syndrome | rel=r_associated | relid=0 | w=26 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 25 / 0.581 -> syndrome de Marfan n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=25 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 21 / 0.488 -> maladie de Marfan n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie de Marfan | rel=r_associated | relid=0 | w=21 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> acanthosis nigricans n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=acanthosis nigricans | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> aclasie diaphysaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=aclasie diaphysaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> acrodermatite entéropathique n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> albinoïdisme n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=albinoïdisme | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> anomalie du développement n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=anomalie du développement | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> arachnodactylie n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=arachnodactylie | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> atrophie optique autosomique dominante n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=atrophie optique autosomique dominante | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> cancer colo-rectal héréditaire sans polypose n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=cancer colo-rectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> cancer colorectal héréditaire sans polypose n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=cancer colorectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> Cancer colorectal héréditaire sans polypose n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=Cancer colorectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> chondrodysplasie déformante héréditaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=chondrodysplasie déformante héréditaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> chondrodysplasie héréditaire déformante n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=chondrodysplasie héréditaire déformante | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> colobome de l'iris avec ptosis, hypertélorisme et retard mental n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=colobome de l'iris avec ptosis, hypertélorisme et retard mental | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> congénital n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=congénital | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> congenital n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=congenital | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> contractures congénitales et arachnodactylie n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> corne cutanée de la paupière n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=corne cutanée de la paupière | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> déficience congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=déficience congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> déformation congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=déformation congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> démence fronto-temporale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> démence frontotemporale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=démence frontotemporale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> difformité congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=difformité congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> dysostose craniofaciale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=dysostose craniofaciale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> dysplasie acromicrique n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> dysplasie cléido-crânienne n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=dysplasie cléido-crânienne | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> dysplasie cléidocrânienne n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=dysplasie cléidocrânienne | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> dysplasie craniodiaphysaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=dysplasie craniodiaphysaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> dystonie dopasensible n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=dystonie dopasensible | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> dystrophie orbitaire congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=dystrophie orbitaire congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> dystrophie papillaire et pigmentaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=dystrophie papillaire et pigmentaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:17q11.2 microduplication syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:absence of fingerprints with congenital milia syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:absence of fingerprints with congenital milia syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:absent corpus callosum n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:absent corpus callosum | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:acro-dermato-ungual-lacrimal-tooth syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:acro-dermato-ungual-lacrimal-tooth syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:acrorenal mandibular syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Alagille's syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Alagille's syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:anauxetic dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:aniridia and intellectual disability syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:aphalangy and syndactyly with microcephaly syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:arachnodactyly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:arterial dissection and lentiginosis syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:arterial dissection and lentiginosis syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:autosomal dominant beta2-microglobulinic amyloidosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant beta2-microglobulinic amyloidosis | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:autosomal dominant charcot-marie-tooth disease type 2m n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant charcot-marie-tooth disease type 2m | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:autosomal dominant focal dystonia dyt25 type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:autosomal dominant palmoplantar keratoderma and congenital alopecia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:bamforth syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:basal cell nævus n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:basal cell nævus | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:basal cell nevus syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:basal cell nevus syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:basal epidermolysis bullosa simplex n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:basal epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Bessel-Hagen's disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Bessel-Hagen's disease | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:bethlem myopathy 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:bethlem myopathy 1 | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:birth defect n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:birth defect | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:bone dysplasia azouz type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:bone dysplasia azouz type | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:brachioskeletogenital syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:brachioskeletogenital syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:cardiac anomaly and heterotaxy syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:cataract glaucoma syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:cervical hypertrichosis and peripheral neuropathy syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:cleidorhizomelic syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cleidorhizomelic syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital anomaly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital defect n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital defect | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:congenital malformation n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:corneal dystrophy, subepithelial mucinous n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:corneal dystrophy, subepithelial mucinous | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:cutaneous photosensitivity and lethal colitis syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:czech dysplasia, metatarsal type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:czech dysplasia, metatarsal type | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:developmental anomaly n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:developmental anomaly | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:developmental fault n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:developmental fault | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:diaphanospondylodysostosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:diaphragmatic hernia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:diaphragmatic hernia | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:diffuse palmoplantar keratoderma and acrocyanosis syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:dyschondrosteosis and nephritis syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:ectodermal dysplasia with blindness syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:ehlers-danlos syndrome vascular-like type n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:epiphyseal dysplasia, multiple, 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:epiphyseal dysplasia, multiple, 2 | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:familial malignant melanoma of skin n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:familial malignant melanoma of skin | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Feingold syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Feingold syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:fountain syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:generalized peeling skin syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:generalized skin thickening (particularly over the trunk) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:generalized skin thickening (particularly over the trunk) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:genetic disorder of skin pigmentation n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:genetic disorder of skin pigmentation | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Gorlin syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Gorlin syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:gracile bone dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hall riggs syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:heart defects limb shortening n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hereditary non polyposis colorectal cancer n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary non polyposis colorectal cancer | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hereditary sensory and autonomic neuropathy type 1b n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary sensory and autonomic neuropathy type 1b | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hyperinsulinism due to hnf1a deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperinsulinism due to hnf1a deficiency | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hyperinsulinism due to insulin receptor deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperinsulinism due to insulin receptor deficiency | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hyperinsulinism due to uncoupling protein 2 deficiency n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hypertrichosis and acromegaloid facial appearance syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypertrichosis and acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hyperuricemia, anemia, renal failure syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperuricemia, anemia, renal failure syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hypohidrosis due to genetic abnormality of eccrine gland structure and function n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypohidrosis due to genetic abnormality of eccrine gland structure and function | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hypomandibular faciocranial dysostosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:hypopigmentation of surgical scars n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hypopigmentation of surgical scars | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:joint hyperextensibility n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:joint hyperextensibility | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:late-onset junctional epidermolysis bullosa n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:lethal larsen-like syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:loose-jointedness n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:loose-jointedness | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Lynch syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Lynch syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Lynch'syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Lynch'syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:major physical defect n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:major physical defect | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Marfan's disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Marfan's syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:morava mehes syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:multiple osteogenic exostoses n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:multiple osteogenic exostoses | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Nathalie syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:non-androgenic hypertrichosis with genetic disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:non-androgenic hypertrichosis with genetic disease | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:nystagmus n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:nystagmus | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:ovarian cysts (in some patients) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:ovarian cysts (in some patients) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:pelviscapular dysplasia n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:physical defect n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:physical defect | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:pili torti onychodysplasia syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:Pitt-Hopkins syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:Pitt-Hopkins syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:piussan lenaerts mathieu syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:preaxial deficiency, postaxial polydactyly and hypospadias n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:primary pigmented nodular adrenocortical disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:primary pigmented nodular adrenocortical disease | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:pterygium colli mental retardation digital anomalies n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:pterygium colli mental retardation digital anomalies | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:robinow-like syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:scholte syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:short fifth metacarpal insulin resistance syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:short fifth metacarpal insulin resistance syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:spinocerebellar ataxia type 32 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia type 32 | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:spinocerebellar ataxia type 37 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spinocerebellar ataxia type 37 | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:split-hand/foot malformation 3 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:telecanthus n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:telecanthus | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:teratosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:teratosis | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:timothy syndrome type 2 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:tubular renal disease with cardiomyopathy syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:von Recklinghausen's disease n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:von Recklinghausen's disease | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability with ataxia and apraxia syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> en:yemenite deaf-blind hypopigmentation syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> exostosante (maladie) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=exostosante (maladie) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> exostose héréditaire multiple n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=exostose héréditaire multiple | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> goniodysgénésie-retard mental-petite taille (syndrome) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=goniodysgénésie-retard mental-petite taille (syndrome) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> hyperkératose nævoïde (hamartomateuse) du mamelon n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=hyperkératose nævoïde (hamartomateuse) du mamelon | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> hyperlaxité ligamentaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=hyperlaxité ligamentaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> hypertélorisme n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=hypertélorisme | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> hypertélorisme-microtie-fente faciale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=hypertélorisme-microtie-fente faciale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> hypertélorisme, hypospadias, polysyndactylie (syndrome) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=hypertélorisme, hypospadias, polysyndactylie (syndrome) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> ichthyose congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=ichthyose congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> Lynch (syndrome de) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=Lynch (syndrome de) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> maladie clinique de recklinghausen n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie clinique de recklinghausen | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> maladie congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> maladie de Bessel-Hagen n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie de Bessel-Hagen | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> maladie de marfan n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie de marfan | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> maladie de Recklinghausen n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie de Recklinghausen | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> maladie de von Recklinghausen n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie de von Recklinghausen | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> maladie des exostoses multiples n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie des exostoses multiples | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> maladie exostosante multiple n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie exostosante multiple | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> maladie ostéogénique n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=maladie ostéogénique | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> malformation congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=malformation congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> migraine hémiplégique familiale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=migraine hémiplégique familiale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> naevomatose baso-cellulaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=naevomatose baso-cellulaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> naevomatose basocellulaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=naevomatose basocellulaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> nævomatose basocellulaire multiple n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=nævomatose basocellulaire multiple | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> nævus dysplasique (syndrome du) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=nævus dysplasique (syndrome du) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neurofibromatose n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neurofibromatose | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neurofibromatose de Recklinghausen n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neurofibromatose de Recklinghausen | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neurofibromatose de recklinghausen n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neurofibromatose de recklinghausen | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neurofibromatose de type 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neurofibromatose de type 1 | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neurofibromatose de type périphérique n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neurofibromatose de type périphérique | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neurofibromatose de type VI n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neurofibromatose de type VI | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neuropathie héréditaire sensitive et autonome de type 1 n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neuropathie héréditaire sensitive et autonome de type 1 | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neuropathie héréditaire sensitive et autonome de type i n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neuropathie héréditaire sensitive et autonome de type i | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neuropathie sensitive héréditaire dominante de type i n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neuropathie sensitive héréditaire dominante de type i | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> neuropathie sensitive héréditaire dominante de type I n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=neuropathie sensitive héréditaire dominante de type I | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> nystagmus congénital isolé n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> onycho-ostéodysostose n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> onycho-patellaire (syndrome) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> pathologie congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> piébaldisme n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=piébaldisme | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> piebaldisme n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=piebaldisme | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> Recklinghausen (maladie de von) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=Recklinghausen (maladie de von) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> Recklinghausen (neurofibromatose de) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=Recklinghausen (neurofibromatose de) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> sclérodermie tubéreuse de bourneville n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=sclérodermie tubéreuse de bourneville | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> sclérose tubéreuse du cerveau n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=sclérose tubéreuse du cerveau | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> stomatocytose héréditaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=stomatocytose héréditaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> syndrome d'Alagille n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome d'Alagille | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> syndrome de douleur extrême paroxystique n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome de douleur extrême paroxystique | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> syndrome de Gorlin n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome de Gorlin | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> syndrome de Lynch n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome de Lynch | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> syndrome de marfan n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> syndrome héréditaire de cancer du sein et de l'ovaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome héréditaire de cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> tare congénitale n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=tare congénitale | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> télécanthus-hypertélorisme-strabisme (syndrome) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=télécanthus-hypertélorisme-strabisme (syndrome) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> tylosis n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=tylosis | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> van Bogaert (xanthomatose cérébrotendineuse de) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> vice de conformation n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=vice de conformation | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> xanthique (lithiase) n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=xanthique (lithiase) | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> xanthomatose cérébro-tendineuse n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse de Van Bogaert n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> xeroderma pigmentosum n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=xeroderma pigmentosum | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> Xeroderma pigmentosum n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=Xeroderma pigmentosum | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) -- r_associated #0: 20 / 0.465 -> xérodermite pigmentaire n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=xérodermite pigmentaire | rel=r_associated | relid=0 | w=20

≈ 809 relations entrantes anomalie congénitale --- r_associated #0: 334 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=anomalie congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=334 en:congenital abnormality --- r_associated #0: 330 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital abnormality | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=330 malformation congénitale --- r_associated #0: 311 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=311 en:congenital defect --- r_associated #0: 310 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital defect | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=310 en:congenital anomaly --- r_associated #0: 309 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital anomaly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=309 déformation congénitale --- r_associated #0: 296 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=déformation congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=296 déficience congénitale --- r_associated #0: 295 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=déficience congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=295 en:marfan syndrome --- r_associated #0: 285 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:marfan syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=285 maladie de Marfan --- r_associated #0: 281 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie de Marfan | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=281 syndrome de Marfan --- r_associated #0: 281 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de Marfan | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=281 arachnodactylie --- r_associated #0: 254 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=arachnodactylie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=254 en:arachnodactyly --- r_associated #0: 234 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:arachnodactyly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=234 difformité congénitale --- r_associated #0: 205 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=difformité congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=205 maladie congénitale --- r_associated #0: 201 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=201 pathologie congénitale --- r_associated #0: 195 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=pathologie congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=195 en:xeroderma pigmentosum --- r_associated #0: 172 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:xeroderma pigmentosum | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=172 xeroderma pigmentosum --- r_associated #0: 170 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xeroderma pigmentosum | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=170 neuropathie héréditaire sensitive et autonome de type 1 --- r_associated #0: 147 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neuropathie héréditaire sensitive et autonome de type 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=147 neuropathie héréditaire sensitive et autonome de type i --- r_associated #0: 145 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neuropathie héréditaire sensitive et autonome de type i | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=145 neuropathie sensitive héréditaire dominante de type i --- r_associated #0: 145 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neuropathie sensitive héréditaire dominante de type i | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=145 en:hereditary sensory autonomic neuropathy, type 1 --- r_associated #0: 143 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary sensory autonomic neuropathy, type 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=143 en:tylosis --- r_associated #0: 131 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:tylosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=131 en:congenital malformation --- r_associated #0: 130 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital malformation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=130 tylosis --- r_associated #0: 130 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=tylosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=130 en:hereditary breast and ovarian cancer syndrome --- r_associated #0: 123 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary breast and ovarian cancer syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=123 en:birth defect --- r_associated #0: 120 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:birth defect | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=120 syndrome héréditaire de cancer du sein et de l'ovaire --- r_associated #0: 120 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome héréditaire de cancer du sein et de l'ovaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=120 syndrome d'Alagille --- r_associated #0: 117 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome d'Alagille | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=117 en:lynch syndrome --- r_associated #0: 116 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:lynch syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=116 démence frontotemporale --- r_associated #0: 115 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=démence frontotemporale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=115 en:Lynch syndrome --- r_associated #0: 115 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Lynch syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=115 syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire --- r_associated #0: 113 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=113 syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire --- r_associated #0: 113 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=113 démence fronto-temporale --- r_associated #0: 112 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=démence fronto-temporale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=112 en:frontotemporal dementia --- r_associated #0: 100 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:frontotemporal dementia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=100 neuropathie sensitive héréditaire dominante de type I --- r_associated #0: 100 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neuropathie sensitive héréditaire dominante de type I | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=100 en:piebaldism --- r_associated #0: 98 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:piebaldism | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=98 hypertélorisme --- r_associated #0: 96 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hypertélorisme | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=96 piebaldisme --- r_associated #0: 95 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=piebaldisme | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=95 piébaldisme --- r_associated #0: 95 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=piébaldisme | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=95 en:hypertelorism --- r_associated #0: 92 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypertelorism | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=92 tare congénitale --- r_associated #0: 85 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=tare congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=85 syndrome de Lynch --- r_associated #0: 81 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de Lynch | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=81 sclérose tubéreuse du cerveau --- r_associated #0: 80 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=sclérose tubéreuse du cerveau | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=80 en:tuberous sclerosis --- r_associated #0: 79 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:tuberous sclerosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=79 congénitale --- r_associated #0: 68 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=68 atrophie optique autosomique dominante --- r_associated #0: 65 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=atrophie optique autosomique dominante | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=65 albinoïdisme --- r_associated #0: 64 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=albinoïdisme | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=64 en:congenital --- r_associated #0: 64 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=64 en:albinoidism --- r_associated #0: 60 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:albinoidism | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=60 vice de conformation --- r_associated #0: 60 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=vice de conformation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=60 congenital --- r_associated #0: 56 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=congenital | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=56 syndrome de Gorlin --- r_associated #0: 56 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de Gorlin | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=56 Xeroderma pigmentosum --- r_associated #0: 55 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Xeroderma pigmentosum | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=55 dysplasie cléidocrânienne --- r_associated #0: 52 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dysplasie cléidocrânienne | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=52 maladie de marfan --- r_associated #0: 52 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie de marfan | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=52 naevomatose baso-cellulaire --- r_associated #0: 52 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=naevomatose baso-cellulaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=52 congénital --- r_associated #0: 51 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=congénital | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=51 maladie de Recklinghausen --- r_associated #0: 51 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie de Recklinghausen | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=51 maladie de von Recklinghausen --- r_associated #0: 51 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie de von Recklinghausen | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=51 neurofibromatose de type 1 --- r_associated #0: 51 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neurofibromatose de type 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=51 xanthomatose cérébro-tendineuse --- r_associated #0: 51 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthomatose cérébro-tendineuse | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=51 xanthomatose cérébrotendineuse --- r_associated #0: 51 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthomatose cérébrotendineuse | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=51 Cancer colorectal héréditaire sans polypose --- r_associated #0: 50 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Cancer colorectal héréditaire sans polypose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=50 acrodermatite entéropathique --- r_associated #0: 50 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=acrodermatite entéropathique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=50 dysplasie cléido-crânienne --- r_associated #0: 50 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dysplasie cléido-crânienne | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=50 en:von Recklinghausen's disease --- r_associated #0: 50 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:von Recklinghausen's disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=50 télécanthus-hypertélorisme-strabisme (syndrome) --- r_associated #0: 50 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télécanthus-hypertélorisme-strabisme (syndrome) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=50 xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 50 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=50 xérodermite pigmentaire --- r_associated #0: 50 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xérodermite pigmentaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=50 Recklinghausen (neurofibromatose de) --- r_associated #0: 49 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Recklinghausen (neurofibromatose de) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=49 maladie clinique de recklinghausen --- r_associated #0: 49 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie clinique de recklinghausen | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=49 en:cerebrotendinous xanthomatosis --- r_associated #0: 48 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cerebrotendinous xanthomatosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=48 en:physical defect --- r_associated #0: 48 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:physical defect | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=48 neurofibromatose de Recklinghausen --- r_associated #0: 48 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neurofibromatose de Recklinghausen | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=48 en:Marfan's syndrome --- r_associated #0: 47 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Marfan's syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=47 en:hereditary nonpolyposis colorectal cancer --- r_associated #0: 47 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary nonpolyposis colorectal cancer | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=47 en:teratosis --- r_associated #0: 47 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:teratosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=47 naevomatose basocellulaire --- r_associated #0: 47 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=naevomatose basocellulaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=47 en:acrodermatitis enteropathica --- r_associated #0: 46 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:acrodermatitis enteropathica | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=46 van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 46 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=46 cancer colo-rectal héréditaire sans polypose --- r_associated #0: 45 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=cancer colo-rectal héréditaire sans polypose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=45 cancer colorectal héréditaire sans polypose --- r_associated #0: 45 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=cancer colorectal héréditaire sans polypose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=45 en:neurofibromatosis --- r_associated #0: 45 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:neurofibromatosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=45 en:major physical defect --- r_associated #0: 44 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:major physical defect | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=44 nystagmus congénital isolé --- r_associated #0: 44 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nystagmus congénital isolé | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=44 en:aphalangy and syndactyly with microcephaly syndrome --- r_associated #0: 43 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=43 en:brachydactyly, type a1 (disorder) --- r_associated #0: 43 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:brachydactyly, type a1 (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=43 en:perniola krajewska carnevale syndrome --- r_associated #0: 43 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:perniola krajewska carnevale syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=43 en:autosomal dominant focal dystonia dyt25 type --- r_associated #0: 42 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=42 en:hereditary papillary renal cell carcinoma --- r_associated #0: 42 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary papillary renal cell carcinoma | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=42 en:nemaline myopathy 3 --- r_associated #0: 42 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:nemaline myopathy 3 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=42 syndrome de douleur extrême paroxystique --- r_associated #0: 42 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de douleur extrême paroxystique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=42 syndrome de marfan --- r_associated #0: 42 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de marfan | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=42 anomalie du développement --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=anomalie du développement | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 en:hawkinsinuria --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hawkinsinuria | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 en:hyperinsulinism due to insulin receptor deficiency --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperinsulinism due to insulin receptor deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 en:li-fraumeni syndrome --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:li-fraumeni syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 en:mesomelic dwarfism reinhardt pfeiffer type --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:mesomelic dwarfism reinhardt pfeiffer type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 en:microphthalmia, syndromic 3 --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:microphthalmia, syndromic 3 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 en:neurofibromatosis type 1 --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:neurofibromatosis type 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 en:paroxysmal extreme pain disorder --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:paroxysmal extreme pain disorder | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 stomatocytose héréditaire --- r_associated #0: 41 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=stomatocytose héréditaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=41 dysostose craniofaciale --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dysostose craniofaciale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 dysostose crânio-faciale --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dysostose crânio-faciale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 en:acrorenal mandibular syndrome --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:acrorenal mandibular syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 en:alpha-fetoprotein, hereditary persistence of --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:alpha-fetoprotein, hereditary persistence of | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 en:charcot-marie-tooth disease, axonal, type 2e (disorder) --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 en:epiphyseal dysplasia, multiple, 2 --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:epiphyseal dysplasia, multiple, 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 en:kbg syndrome --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:kbg syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 en:pseudohypoaldosteronism, type 1, dominant form --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pseudohypoaldosteronism, type 1, dominant form | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 en:spinocerebellar ataxia 8 --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia 8 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 onycho-ostéodysostose --- r_associated #0: 40 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=onycho-ostéodysostose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=40 en:anauxetic dysplasia --- r_associated #0: 39 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:anauxetic dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=39 en:corneal dystrophy, congenital stromal --- r_associated #0: 39 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:corneal dystrophy, congenital stromal | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=39 en:hereditary stomatocytosis --- r_associated #0: 39 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary stomatocytosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=39 goniodysgénésie-retard mental-petite taille (syndrome) --- r_associated #0: 39 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=goniodysgénésie-retard mental-petite taille (syndrome) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=39 hypertélorisme, hypospadias, polysyndactylie (syndrome) --- r_associated #0: 39 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hypertélorisme, hypospadias, polysyndactylie (syndrome) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=39 hypertélorisme-microtie-fente faciale --- r_associated #0: 39 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hypertélorisme-microtie-fente faciale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=39 neurofibromatose de type VI --- r_associated #0: 39 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neurofibromatose de type VI | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=39 nævomatose basocellulaire multiple --- r_associated #0: 39 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nævomatose basocellulaire multiple | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=39 dysplasie acromicrique --- r_associated #0: 38 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dysplasie acromicrique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=38 dystrophie orbitaire congénitale --- r_associated #0: 38 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dystrophie orbitaire congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=38 en:basal cell nevus syndrome --- r_associated #0: 38 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:basal cell nevus syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=38 en:familial isolated arrhythmogenic right ventricular dysplasia --- r_associated #0: 38 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial isolated arrhythmogenic right ventricular dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=38 en:zimmerman laband syndrome --- r_associated #0: 38 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:zimmerman laband syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=38 en:syndactyly, type iii --- r_associated #0: 37 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:syndactyly, type iii | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=37 en:Lynch'syndrome --- r_associated #0: 36 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Lynch'syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=36 en:angioma hereditary neurocutaneous --- r_associated #0: 36 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:angioma hereditary neurocutaneous | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=36 en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 36 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=36 en:craniofacial dysostosis --- r_associated #0: 36 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:craniofacial dysostosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=36 en:hereditary angioedema --- r_associated #0: 36 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary angioedema | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=36 en:nail-patella syndrome --- r_associated #0: 36 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:nail-patella syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=36 en:sebastian syndrome --- r_associated #0: 36 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:sebastian syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=36 neurofibromatose de type périphérique --- r_associated #0: 36 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neurofibromatose de type périphérique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=36 Syndrome de Marfan --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Syndrome de Marfan | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:angiokeratoma corporis diffusum --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:angiokeratoma corporis diffusum | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:autosomal dominant ichthyosis vulgaris --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant ichthyosis vulgaris | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:avascular necrosis of femoral head --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:avascular necrosis of femoral head | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:basal epidermolysis bullosa simplex --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:basal epidermolysis bullosa simplex | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:behavioral variant of frontotemporal dementia --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:behavioral variant of frontotemporal dementia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:brachyolmia type 3 --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:brachyolmia type 3 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:cap myopathy --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cap myopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:chromosome 17q21.31 deletion syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:chromosome 22q11.2 microduplication syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:chromosome 22q11.2 microduplication syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:congenital ichthyosis --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital ichthyosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:crouzon syndrome with acanthosis nigricans, ala391glu (allelic variant) --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:crouzon syndrome with acanthosis nigricans, ala391glu (allelic variant) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:epithelial recurrent erosion dystrophy --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:epithelial recurrent erosion dystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:familial amyloid polyneuropathy with cutaneous amyloidosis --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial amyloid polyneuropathy with cutaneous amyloidosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:farber lipogranulomatosis --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:farber lipogranulomatosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:fibular hypoplasia and complex brachydactyly --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:fibular hypoplasia and complex brachydactyly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:frontotemporal dementia, chromosome 3-linked --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:frontotemporal dementia, chromosome 3-linked | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:hand foot uterus syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hand foot uterus syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:hereditary cystatin c amyloid angiopathy --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary cystatin c amyloid angiopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:hereditary elliptocytosis due to alpha spectrin defect --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary elliptocytosis due to alpha spectrin defect | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:hyperinsulinism due to hnf1a deficiency --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperinsulinism due to hnf1a deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:hypopigmentation of surgical scars --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypopigmentation of surgical scars | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:lissencephaly syndrome, norman-roberts type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:morquio syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:morquio syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:neurofibromatosis type 2 --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:neurofibromatosis type 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:neuropathy, hereditary thermosensitive --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:neuropathy, hereditary thermosensitive | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:nevoid basal cell carcinoma syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:nevoid basal cell carcinoma syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:pili torti onychodysplasia syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pili torti onychodysplasia syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:pitt-hopkins syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pitt-hopkins syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:potocki-shaffer syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:potocki-shaffer syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:reardon hall slaney syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:reardon hall slaney syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:rhizomelic chondrodysplasia punctata --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:rhizomelic chondrodysplasia punctata | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:rothmund-thomson syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:rothmund-thomson syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:scholte syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:scholte syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:spinocerebellar ataxia type 2 --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia type 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:spinocerebellar ataxia type 32 --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia type 32 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:split-hand-foot malformation with long bone deficiency 1 --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:split-hand-foot malformation with long bone deficiency 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:spondylocostal dysostosis 4, autosomal dominant --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:steinfeld syndrome --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:steinfeld syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:sting-associated vasculopathy with onset in infancy --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:sting-associated vasculopathy with onset in infancy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:syndactyly, type i --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:syndactyly, type i | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:timothy syndrome type 2 --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:timothy syndrome type 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 en:vitelliform macular dystrophy --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:vitelliform macular dystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 hyperlaxité ligamentaire --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperlaxité ligamentaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 ichthyose congénitale --- r_associated #0: 35 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=ichthyose congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=35 dysostose crâniofaciale --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dysostose crâniofaciale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:17q11.2 microduplication syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:17q11.2 microduplication syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:Marfan's disease --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Marfan's disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:acanthosis nigricans of oral mucous membranes --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:acanthosis nigricans of oral mucous membranes | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:acromicric dysplasia --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:acromicric dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:aniridia and intellectual disability syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:aniridia and intellectual disability syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:autosomal dominant charcot-marie-tooth disease type 2m --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant charcot-marie-tooth disease type 2m | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:autosomal dominant deficiency of plasminogen --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant deficiency of plasminogen | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:bethlem myopathy 1 --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:bethlem myopathy 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:bone dysplasia azouz type --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:bone dysplasia azouz type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:brachymesophalangy 2 and 5 --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:brachymesophalangy 2 and 5 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:charcot-marie-tooth disease, type 2j --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:charcot-marie-tooth disease, type 2j | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:cole disease --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cole disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:dicer1 syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dicer1 syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:dysplasia, saddan --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dysplasia, saddan | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:glomuvenous malformations --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:glomuvenous malformations | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:hall riggs syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hall riggs syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:heart defects limb shortening --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:heart defects limb shortening | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:hereditary gastrogenic lactose intolerance --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary gastrogenic lactose intolerance | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:hereditary sensory and autonomic neuropathy type 1b --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary sensory and autonomic neuropathy type 1b | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:heritable pulmonary arterial hypertension due to bmpr2 mutation --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:hyperinsulinism due to uncoupling protein 2 deficiency --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:hyperpigmentation, familial progressive --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperpigmentation, familial progressive | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:hypertrichosis and acromegaloid facial appearance syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypertrichosis and acromegaloid facial appearance syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:inherited arthrogryposis --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:inherited arthrogryposis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:late-onset junctional epidermolysis bullosa --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:late-onset junctional epidermolysis bullosa | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:loose-jointedness --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:loose-jointedness | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:majeed syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:majeed syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:microcephaly cervical spine fusion anomalies --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:microcephaly cervical spine fusion anomalies | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:microcephaly deafness syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:microcephaly deafness syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:microcornea with glaucoma and absent frontal sinus syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:microcornea with glaucoma and absent frontal sinus syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:multiple endocrine neoplasia type 2b --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:multiple endocrine neoplasia type 2b | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:myopathy with abnormal lipid metabolism --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:myopathy with abnormal lipid metabolism | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:nonaka myopathy --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:nonaka myopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:noonan syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:noonan syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:peeling skin syndrome, acral type --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:peeling skin syndrome, acral type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:pili torti-deafness syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pili torti-deafness syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:pseudocholinesterase deficiency --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pseudocholinesterase deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:robinow-like syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:robinow-like syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:spinocerebellar ataxia 1s --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia 1s | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:spinocerebellar ataxia 36 --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia 36 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:split-hand/foot malformation 3 --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:split-hand/foot malformation 3 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:ulna metaphyseal dysplasia syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ulna metaphyseal dysplasia syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:ulnar-mammary syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ulnar-mammary syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability with ataxia and apraxia syndrome --- r_associated #0: 34 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34 dystonie dopasensible --- r_associated #0: 33 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dystonie dopasensible | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=33 onycho-patellaire (syndrome) --- r_associated #0: 33 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=onycho-patellaire (syndrome) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=33 dysplasie craniodiaphysaire --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dysplasie craniodiaphysaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:autosomal dominant muscular dystrophy not predominantly limb girdle --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant muscular dystrophy not predominantly limb girdle | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:bilateral pheochromocytoma and islet cell adenoma of the pancreas --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:charcot-marie-tooth disease type 2d --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:charcot-marie-tooth disease type 2d | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:charcot-marie-tooth disease, axonal, type 2b (disorder) --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:chondrodysplasia punctata syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:chondrodysplasia punctata syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:chromosome 3q29 deletion syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:chromosome 3q29 deletion syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:cleidocranial dysplasia --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cleidocranial dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:congenital craniofacial dysostosis --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital craniofacial dysostosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:diffuse palmoplantar keratoderma and acrocyanosis syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:dominant autosomal hereditary disorder, incomplete penetrance --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dominant autosomal hereditary disorder, incomplete penetrance | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:dopa-responsive dystonia --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dopa-responsive dystonia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:dysplastic nevus syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dysplastic nevus syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:episodic ataxia --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:episodic ataxia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:familial cold autoinflammatory syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial cold autoinflammatory syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:familial osteochondritis dissecans --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial osteochondritis dissecans | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:familial partial lipodystrophy, type 2 --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial partial lipodystrophy, type 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:fibrodysplasia ossificans progressiva --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:fibrodysplasia ossificans progressiva | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:fronto-facio-nasal dysplasia --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:fronto-facio-nasal dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:generalized epilepsy and paroxysmal dyskinesia syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:generalized epilepsy and paroxysmal dyskinesia syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:glycogen storage disease 0, liver --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:glycogen storage disease 0, liver | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:hereditary non polyposis colorectal cancer --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary non polyposis colorectal cancer | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:holoprosencephaly with fetal akinesia-hypokinesia sequence --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:hypohidrosis due to genetic abnormality of eccrine gland structure and function --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypohidrosis due to genetic abnormality of eccrine gland structure and function | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:hypomandibular faciocranial dysostosis --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypomandibular faciocranial dysostosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:iris coloboma with ptosis, hypertelorism, and mental retardation --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:iris coloboma with ptosis, hypertelorism, and mental retardation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:knobloch syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:knobloch syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:non-androgenic hypertrichosis with genetic disease --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:non-androgenic hypertrichosis with genetic disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:pituitary adenoma, familial isolated (disorder) --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pituitary adenoma, familial isolated (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:potassium aggravated myotonia --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:potassium aggravated myotonia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:preaxial deficiency, postaxial polydactyly and hypospadias --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:short fifth metacarpal insulin resistance syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:short fifth metacarpal insulin resistance syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:shprintzen omphalocele syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:shprintzen omphalocele syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:smith-mccort dysplasia --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:smith-mccort dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:spinocerebellar ataxia type 4 --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia type 4 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:spondyloenchondrodysplasia --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondyloenchondrodysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:spondyloepiphyseal dysplasia, omani type --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondyloepiphyseal dysplasia, omani type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:spondyloperipheral dysplasia short ulna --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondyloperipheral dysplasia short ulna | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:syndrome, branchio-oculo-facial --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:syndrome, branchio-oculo-facial | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:verloes bourguignon syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:verloes bourguignon syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:von hippel-lindau syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:von hippel-lindau syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 exostosante (maladie) --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=exostosante (maladie) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 nævus dysplasique (syndrome du) --- r_associated #0: 32 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nævus dysplasique (syndrome du) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:ameloonychohypohidrotic syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ameloonychohypohidrotic syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:autosomal dominant charcot-marie-tooth disease type 2c --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant charcot-marie-tooth disease type 2c | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:autosomal dominant oculocutaneous albinism --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant oculocutaneous albinism | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:bamforth syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:bamforth syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:benign autosomal dominant osteopetrosis --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:benign autosomal dominant osteopetrosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:craniodiaphyseal dysplasia --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:craniodiaphyseal dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:cutis laxa, autosomal recessive --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cutis laxa, autosomal recessive | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:dystonia 12 --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dystonia 12 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ectodermal dysplasia with blindness syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:familial malignant melanoma of skin --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial malignant melanoma of skin | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:fountain syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:fountain syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:giacci familial neurogenic acroosteolysis --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:giacci familial neurogenic acroosteolysis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:glycogen storage disease type x --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:glycogen storage disease type x | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:hereditary systemic amyloidosis --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary systemic amyloidosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:hyperinsulinism due to deficiency of glucokinase --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperinsulinism due to deficiency of glucokinase | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:leopard syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:leopard syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:liddle syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:liddle syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:melanoma astrocytoma syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:melanoma astrocytoma syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:myopathy with exercise intolerance, swedish type --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:myopathy with exercise intolerance, swedish type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:ocular albinism-lentigines-deafness syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ocular albinism-lentigines-deafness syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:partington x-linked mental retardation syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:partington x-linked mental retardation syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:piussan lenaerts mathieu syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:piussan lenaerts mathieu syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:radial hypoplasia, triphalangeal thumbs and hypospadias --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:radial hypoplasia, triphalangeal thumbs and hypospadias | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:robinow syndrome --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:robinow syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:synpolydactyly --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:synpolydactyly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:telecanthus --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:telecanthus | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 en:wnt4 mullerian aplasia and ovarian dysfunction --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:wnt4 mullerian aplasia and ovarian dysfunction | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 migraine hémiplégique familiale --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=migraine hémiplégique familiale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 neurofibromatose --- r_associated #0: 31 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neurofibromatose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=31 Syndrome d'Alagille --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Syndrome d'Alagille | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 Syndrome de Gorlin --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Syndrome de Gorlin | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 aclasie diaphysaire --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=aclasie diaphysaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 chondrodysplasie déformante héréditaire --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=chondrodysplasie déformante héréditaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 chondrodysplasie héréditaire déformante --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=chondrodysplasie héréditaire déformante | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 contractures congénitales et arachnodactylie --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=contractures congénitales et arachnodactylie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 corne cutanée de la paupière --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=corne cutanée de la paupière | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:Alagille's syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Alagille's syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:Feingold syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Feingold syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:Gorlin syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Gorlin syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:Nathalie syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Nathalie syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:Pitt-Hopkins syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Pitt-Hopkins syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:absent corpus callosum --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:absent corpus callosum | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:alagille syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:alagille syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:autosomal dominant excess of transthyretin --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant excess of transthyretin | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:autosomal dominant progressive nephropathy with hypertension --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant progressive nephropathy with hypertension | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal recessive distal osteolysis syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:beare-stevenson cutis gyrata syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:brachydactyly type a6 --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:brachydactyly type a6 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:capillary malformation-arteriovenous malformation (disorder) --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:capillary malformation-arteriovenous malformation (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dentatorubral-pallidoluysian atrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:developmental fault --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:developmental fault | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:dyskeratosis congenita, autosomal dominant --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dyskeratosis congenita, autosomal dominant | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:ectodermal dysplasia with natal teeth, turnpenny type --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ectodermal dysplasia with natal teeth, turnpenny type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:familial arthrogryposis-cholestatic hepatorenal syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial arthrogryposis-cholestatic hepatorenal syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:familial encephalopathy with neuroserpin inclusion bodies --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial encephalopathy with neuroserpin inclusion bodies | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:familial non-autoimmune autosomal dominant hyperthyroidism --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial non-autoimmune autosomal dominant hyperthyroidism | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:generalized myotonia of thomsen --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:generalized myotonia of thomsen | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:generalized skin thickening (particularly over the trunk) --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:generalized skin thickening (particularly over the trunk) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:genetic disorder of skin pigmentation --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:genetic disorder of skin pigmentation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:haspeslagh fryns muelenaere syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:hereditary multiple exostoses --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary multiple exostoses | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:hyaline dystrophy of bruch's membrane --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyaline dystrophy of bruch's membrane | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:hyperferritinemia, hereditary, with congenital cataracts --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:hypermobility syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypermobility syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:hyperparathyroidism-jaw tumor syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperparathyroidism-jaw tumor syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:hyperuricemia, anemia, renal failure syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperuricemia, anemia, renal failure syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:jackson-weiss syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:jackson-weiss syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:laurin-sandrow syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:laurin-sandrow syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:mullerian duct and limb anomalies syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:mullerian duct and limb anomalies syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:multiple osteogenic exostoses --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:multiple osteogenic exostoses | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:muscle l-lactate dehydrogenase deficiency --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:muscle l-lactate dehydrogenase deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:okihiro syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:okihiro syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:primary pigmented nodular adrenocortical disease --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:primary pigmented nodular adrenocortical disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:pterygium colli mental retardation digital anomalies --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pterygium colli mental retardation digital anomalies | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:roch leri mesosomatous lipomatosis --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:roch leri mesosomatous lipomatosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:sellars beighton syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:sellars beighton syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:spinocerebellar ataxia type 6 (disorder) --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia type 6 (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 en:wellesley carman french syndrome --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:wellesley carman french syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 exostose héréditaire multiple --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=exostose héréditaire multiple | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 maladie de Bessel-Hagen --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie de Bessel-Hagen | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 maladie des exostoses multiples --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie des exostoses multiples | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 maladie exostosante multiple --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie exostosante multiple | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 maladie ostéogénique --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=maladie ostéogénique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 neurofibromatose de recklinghausen --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neurofibromatose de recklinghausen | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 sclérodermie tubéreuse de bourneville --- r_associated #0: 30 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=sclérodermie tubéreuse de bourneville | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=30 Lynch (syndrome de) --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Lynch (syndrome de) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 colobome de l'iris avec ptosis, hypertélorisme et retard mental --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=colobome de l'iris avec ptosis, hypertélorisme et retard mental | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:Bessel-Hagen's disease --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Bessel-Hagen's disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:acrodysostosis --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:acrodysostosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:acute intermittent porphyria --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:acute intermittent porphyria | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:advanced sleep-phase syndrome, familial --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:advanced sleep-phase syndrome, familial | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:arthrogryposis, distal, type 1 --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:arthrogryposis, distal, type 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:ataxia telangiectasia syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ataxia telangiectasia syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:auriculo-condylar syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:auriculo-condylar syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:autosomal dominant familial woolly hair --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant familial woolly hair | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:autosomal dominant pterygium of conjunctiva --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant pterygium of conjunctiva | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:baller-gerold syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:baller-gerold syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:brachioskeletogenital syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:brachioskeletogenital syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:brooke-spiegler syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:brooke-spiegler syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:cataract, congenital, cerulean type 1 --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cataract, congenital, cerulean type 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:cerebral cavernous malformation --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cerebral cavernous malformation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:char syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:char syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:charcot-marie-tooth disease, axonal, type 2l (disorder) --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:chronic infantile neurological cutaneous and articular syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:chronic infantile neurological cutaneous and articular syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:cutis laxa, autosomal dominant --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cutis laxa, autosomal dominant | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:czech dysplasia, metatarsal type --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:czech dysplasia, metatarsal type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:distal arthrogryposis syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:distal arthrogryposis syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:ehlers-danlos syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ehlers-danlos syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:familial amyloid polyneuropathy, type v --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial amyloid polyneuropathy, type v | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:familial benign neonatal epilepsy --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial benign neonatal epilepsy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:geniospasm 1 --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:geniospasm 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:glucose transporter protein type 1 deficiency syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:glucose transporter protein type 1 deficiency syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:hallermann syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hallermann syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:hereditary elliptocytosis due to abnormal protein 4.1 --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary elliptocytosis due to abnormal protein 4.1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:hereditary elliptocytosis due to beta spectrin defect in self-association --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary elliptocytosis due to beta spectrin defect in self-association | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:hnsha due to triosephosphate isomerase deficiency --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hnsha due to triosephosphate isomerase deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:hyperinsulinemic hypoglycemia, familial, 6 --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperinsulinemic hypoglycemia, familial, 6 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:hyperinsulinemic hypoglycemia, familial, 7 --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperinsulinemic hypoglycemia, familial, 7 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:insulin autoimmune syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:insulin autoimmune syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:klippel-feil syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:klippel-feil syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:macular corneal dystrophy --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:macular corneal dystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:metaphyseal dysplasia, braun-tinschert type --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:metaphyseal dysplasia, braun-tinschert type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:myopathy, distal 2 --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:myopathy, distal 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:nathalie syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:nathalie syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:neurofibromatosis, type 1-like syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:neurofibromatosis, type 1-like syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:neuropathy, hereditary motor and sensory, okinawa type --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:neuropathy, hereditary motor and sensory, okinawa type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:papillon-lefevre syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:papillon-lefevre syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:peutz-jeghers syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:peutz-jeghers syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:polydactyly, preaxial ii (disorder) --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:polydactyly, preaxial ii (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:reticulate acropigmentation of kitamura --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:reticulate acropigmentation of kitamura | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:short stature with valvular heart disease and characteristic facies syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:short stature with valvular heart disease and characteristic facies syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:sitosterolemia with xanthomatosis --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:sitosterolemia with xanthomatosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:spinocerebellar ataxia 29 --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia 29 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:spondylo-ocular syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondylo-ocular syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:transthyretin related familial amyloid cardiomyopathy --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:transthyretin related familial amyloid cardiomyopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:triglyceride storage disease with ichthyosis --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:triglyceride storage disease with ichthyosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:turcot syndrome --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:turcot syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:whyte hemingway carpal tarsal phalangeal osteolyses --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:whyte hemingway carpal tarsal phalangeal osteolyses | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 syndrome de gorlin --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de gorlin | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 xanthique (lithiase) --- r_associated #0: 29 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthique (lithiase) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:absence of fingerprints with congenital milia syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:absence of fingerprints with congenital milia syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:aplasia of lacrimal and salivary glands --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:aplasia of lacrimal and salivary glands | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:autosomal dominant charcot-marie-tooth disease type 2a1 --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant charcot-marie-tooth disease type 2a1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:bannayan syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:bannayan syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:benign congenital myopathy --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:benign congenital myopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:brody myopathy --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:brody myopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:cataract glaucoma syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cataract glaucoma syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:choreoathetosis/spasticity, episodic --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:choreoathetosis/spasticity, episodic | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:cleidorhizomelic syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cleidorhizomelic syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:cochleosaccular degeneration of the inner ear and progressive cataracts --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:corneal dystrophy, subepithelial mucinous --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:corneal dystrophy, subepithelial mucinous | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:disseminated superficial porokeratosis --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:disseminated superficial porokeratosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:dominant autosomal hereditary disorder, complete penetrance --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dominant autosomal hereditary disorder, complete penetrance | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:dominant beta-thalassemia --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dominant beta-thalassemia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:dyskeratosis congenita --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dyskeratosis congenita | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ehlers-danlos syndrome vascular-like type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:familial acantholysis --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial acantholysis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:familial hemiplegic migraine --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial hemiplegic migraine | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:familial hypercalciuric hypocalcemia --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial hypercalciuric hypocalcemia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:familial hypodontia --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial hypodontia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:familial spontaneous pneumothorax --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial spontaneous pneumothorax | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:fleck corneal dystrophy --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:fleck corneal dystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:freeman-sheldon syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:freeman-sheldon syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:gracile bone dysplasia --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:gracile bone dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:gurrieri sammito bellussi syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:gurrieri sammito bellussi syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:hypotrichosis simplex of scalp --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypotrichosis simplex of scalp | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:keratosis palmoplantaris papulosa --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:keratosis palmoplantaris papulosa | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:klippel-trenaunay-weber syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:klippel-trenaunay-weber syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:kuskokwim disease --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:kuskokwim disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:lethal congenital contracture syndrome 1 --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:lethal congenital contracture syndrome 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:morava mehes syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:morava mehes syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:mowat-wilson syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:mowat-wilson syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:multiple self healing epithelioma of ferguson-smith --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:multiple self healing epithelioma of ferguson-smith | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:muscle amp deaminase deficiency --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:muscle amp deaminase deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:ovarian cysts (in some patients) --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ovarian cysts (in some patients) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:parietal foramina --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:parietal foramina | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:premature aging syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:premature aging syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:pulmonary interstitial glycogenosis --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pulmonary interstitial glycogenosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:reis-bucklers' corneal dystrophy --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:reis-bucklers' corneal dystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:spinocerebellar ataxia 10 --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia 10 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:spinocerebellar ataxia 28 --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia 28 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:spinocerebellar ataxia 31 (disorder) --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia 31 (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:spondyloenchondrodysplasia with immune dysregulation --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:spondyloepiphyseal dysplasia tarda, x-linked --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondyloepiphyseal dysplasia tarda, x-linked | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:treacher collins syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:treacher collins syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:type i acrocephalosyndactyly --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:type i acrocephalosyndactyly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:type v acrocephalosyndactyly --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:type v acrocephalosyndactyly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:vitreoretinochoroidopathy (disorder) --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:vitreoretinochoroidopathy (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:von willebrand disease, platelet type --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:von willebrand disease, platelet type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 en:wells jankovic syndrome --- r_associated #0: 28 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:wells jankovic syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=28 Maladie congénitale --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Maladie congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 Recklinghausen (maladie de von) --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Recklinghausen (maladie de von) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 dystrophie papillaire et pigmentaire --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=dystrophie papillaire et pigmentaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:antley-bixler syndrome, autosomal dominant | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:arterial dissection and lentiginosis syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:arterial dissection and lentiginosis syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:atelosteogenesis, type 1 --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:atelosteogenesis, type 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:atrophoderma vermiculatum --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:atrophoderma vermiculatum | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:autosomal dominant analbuminemia --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant analbuminemia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:autosomal dominant mutilating keratoderma --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant mutilating keratoderma | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:autosomal dominant optic atrophy --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant optic atrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:autosomal dominant palmoplantar keratoderma and congenital alopecia --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:autosomal dominant polycystic kidney disease --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant polycystic kidney disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:cerebral hemorrhage with amyloidosis, hereditary, dutch type --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:congenital bowing of long bone --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital bowing of long bone | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:congenital reticular ichthyosiform erythroderma --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital reticular ichthyosiform erythroderma | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:craniofacial deafness hand syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:craniofacial deafness hand syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:deafness-craniofacial syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:deafness-craniofacial syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:developmental anomaly --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:developmental anomaly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:diaphragmatic hernia --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:diaphragmatic hernia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:dysostosis multiplex group --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dysostosis multiplex group | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:epilepsy, myoclonic, benign adult familial, type 2 --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:epilepsy, myoclonic, benign adult familial, type 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:epiphyseal dysplasia, multiple, 1 --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:epiphyseal dysplasia, multiple, 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:familial creutzfeldt-jakob --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial creutzfeldt-jakob | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:feingold syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:feingold syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:generalized peeling skin syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:generalized peeling skin syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:geroderma osteodysplastica --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:geroderma osteodysplastica | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:heide syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:heide syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:hereditary diffuse gastric adenocarcinoma --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary diffuse gastric adenocarcinoma | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:hereditary myopathy with early respiratory failure --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary myopathy with early respiratory failure | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:keratoacanthoma familial --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:keratoacanthoma familial | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:lethal congenital contracture syndrome type 3 --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:lethal congenital contracture syndrome type 3 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:lethal larsen-like syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:lethal larsen-like syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:lipoid proteinosis of urbach and wiethe | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:macdermot winter syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:macdermot winter syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:marden-walker syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:marden-walker syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:may-hegglin anomaly --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:may-hegglin anomaly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:multiple epiphyseal dysplasia type 5 --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:multiple epiphyseal dysplasia type 5 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:myopathy, distal, tateyama type --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:myopathy, distal, tateyama type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:naxos disease --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:naxos disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:osteogenesis imperfecta, levin type --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:osteogenesis imperfecta, levin type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:palmoplantar porokeratosis --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:palmoplantar porokeratosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:polyostotic fibrous dysplasia --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:polyostotic fibrous dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:primary hypertrophic osteoarthropathy --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:primary hypertrophic osteoarthropathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:proteus-like syndrome (disorder) --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:proteus-like syndrome (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:schinzel-giedion midface-retraction syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:schinzel-giedion midface-retraction syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:spinocerebellar ataxia type 5 --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia type 5 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:stickler syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:stickler syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:strudwick syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:strudwick syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:tarsal-carpal coalition syndrome --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:tarsal-carpal coalition syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:thiel-behnke corneal dystrophy --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:thiel-behnke corneal dystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 en:type ii acrocephalopolysyndactyly --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:type ii acrocephalopolysyndactyly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 hyperkératose nævoïde (hamartomateuse) du mamelon --- r_associated #0: 27 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperkératose nævoïde (hamartomateuse) du mamelon | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=27 acanthosis nigricans --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=acanthosis nigricans | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:acanthosis nigricans --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:acanthosis nigricans | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:acro-dermato-ungual-lacrimal-tooth syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:acro-dermato-ungual-lacrimal-tooth syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:adult onset autosomal dominant leukodystrophy --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:adult onset autosomal dominant leukodystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:amelogenesis imperfecta, type ib --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:amelogenesis imperfecta, type ib | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:autosomal dominant beta2-microglobulinic amyloidosis --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant beta2-microglobulinic amyloidosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:autosomal dominant hyperinsulinism due to kir6.2 deficiency --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:autosomal dominant hyperinsulinism due to sur1 deficiency --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant hyperinsulinism due to sur1 deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:autosomal dominant idiopathic familial dystonia --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant idiopathic familial dystonia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:autosomal dominant late onset basal ganglia degeneration --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant late onset basal ganglia degeneration | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:autosomal dominant variant form of albumin --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant variant form of albumin | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:basal cell nævus --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:basal cell nævus | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:bilateral multiple fibroadenoma of breast --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:bilateral multiple fibroadenoma of breast | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:blau syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:blau syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:centronuclear myopathy 1 --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:centronuclear myopathy 1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:congenital dyserythropoietic anemia, type iii --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital dyserythropoietic anemia, type iii | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:congenital nephrogenic diabetes insipidus --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital nephrogenic diabetes insipidus | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:congenital premature fusion --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital premature fusion | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:currarino triad --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:currarino triad | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:cystinosis, infantile nephropathic --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cystinosis, infantile nephropathic | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:diaphanospondylodysostosis --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:diaphanospondylodysostosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dyschondrosteosis and nephritis syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:dystrophia myotonica 2 --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dystrophia myotonica 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:familial amyloid neuropathy --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial amyloid neuropathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:familial digital arthropathy and brachydactyly syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial digital arthropathy and brachydactyly syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:familial interstitial nephritis --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:familial interstitial nephritis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:follicular atrophoderma and basal cell epitheliomata --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:follicular atrophoderma and basal cell epitheliomata | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:genitopatellar syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:genitopatellar syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:glycogen storage disease, muscular form --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:glycogen storage disease, muscular form | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:hereditary motor and sensory neuropathy type i --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary motor and sensory neuropathy type i | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:hereditary mucosal leukokeratosis --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary mucosal leukokeratosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:hereditary tubulointerstitial disorder --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary tubulointerstitial disorder | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:hyperinsulinism due to hnf4a deficiency --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperinsulinism due to hnf4a deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:hypoplastic tibia and postaxial polydactyly syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypoplastic tibia and postaxial polydactyly syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:joint hyperextensibility --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:joint hyperextensibility | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:lamellar ichthyosis, autosomal dominant form --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:lamellar ichthyosis, autosomal dominant form | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:lethal congenital contracture syndrome 2 --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:lethal congenital contracture syndrome 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:melnick-fraser syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:melnick-fraser syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:menkes disease --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:menkes disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:muckle-wells syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:muckle-wells syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:nicolaides baraitser syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:nicolaides baraitser syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:non-dystrophic myotonia --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:non-dystrophic myotonia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:nystagmus --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:nystagmus | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:oculocutaneous albinism --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:oculocutaneous albinism | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:otoonychoperoneal syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:otoonychoperoneal syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:pelviscapular dysplasia --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pelviscapular dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:peripheral resistance to thyroid hormone --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:peripheral resistance to thyroid hormone | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:poikiloderma, hereditary sclerosing --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:poikiloderma, hereditary sclerosing | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:popliteal pterygium syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:popliteal pterygium syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:prune belly syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:prune belly syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:saito kuba tsuruta syndrome --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:saito kuba tsuruta syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:spinocerebellar ataxia type 37 --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia type 37 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:spinocerebellar ataxia type 7 --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spinocerebellar ataxia type 7 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:spondylocamptodactyly --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:spondylocamptodactyly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:steatocystoma multiplex --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:steatocystoma multiplex | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:syndromic orbital border hypoplasia --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:syndromic orbital border hypoplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 26 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=26 en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:autoimmune lymphoproliferative syndrome --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autoimmune lymphoproliferative syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:autosomal dominant epidermolysis bullosa simplex --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant epidermolysis bullosa simplex | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:becker generalized myotonia --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:becker generalized myotonia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:clinical significant laxity --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:clinical significant laxity | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:ehlers-danlos syndrome, type i --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ehlers-danlos syndrome, type i | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:femur bifid with monodactylous ectrodactyly --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:femur bifid with monodactylous ectrodactyly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:foxg1 syndrome --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:foxg1 syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:hereditary oculoleptomeningeal amyloid angiopathy --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:radial aplasia-thrombocytopenia syndrome --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:radial aplasia-thrombocytopenia syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:strabismus syndrome --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:strabismus syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 malformation --- r_associated #0: 25 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=25 en:andersen syndrome --- r_associated #0: 24 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:andersen syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=24 en:arachnodactily --- r_associated #0: 24 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:arachnodactily | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=24 en:autosomal dominant retinitis pigmentosa --- r_associated #0: 24 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant retinitis pigmentosa | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=24 en:congenital hereditary muscular dystrophy --- r_associated #0: 24 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:congenital hereditary muscular dystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=24 en:dentin dyspalsia, shields type 2 --- r_associated #0: 24 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dentin dyspalsia, shields type 2 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=24 en:hereditary benign intraepithelial dyskeratosis --- r_associated #0: 24 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary benign intraepithelial dyskeratosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=24 en:hereditary hemorrhagic telangiectasia --- r_associated #0: 24 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary hemorrhagic telangiectasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=24 en:zinc-deficiency type --- r_associated #0: 24 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:zinc-deficiency type | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=24 tylose --- r_associated #0: 24 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=tylose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=24 acrodermatitis enteropathica --- r_associated #0: 23 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=acrodermatitis enteropathica | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=23 chondrodysplasie rhizomélique ponctuée --- r_associated #0: 23 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=chondrodysplasie rhizomélique ponctuée | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=23 en:excessive joint laxity --- r_associated #0: 23 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:excessive joint laxity | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=23 en:hereditary elliptocytosis due to deficiency of protein 4.1 --- r_associated #0: 23 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary elliptocytosis due to deficiency of protein 4.1 | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=23 en:onychoosteodysostosis --- r_associated #0: 23 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:onychoosteodysostosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=23 en:shwachman-diamond syndrome --- r_associated #0: 23 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:shwachman-diamond syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=23 télécanthus --- r_associated #0: 23 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télécanthus | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=23 en:acquired acanthosis nigricans --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:acquired acanthosis nigricans | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 en:autosomal dominant cystoid macular edema --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant cystoid macular edema | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 en:brachydactyly syndrome type b --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:brachydactyly syndrome type b | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 en:keratitis, hereditary --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:keratitis, hereditary | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 en:kohlschutter tonz syndrome --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:kohlschutter tonz syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 en:pyle metaphyseal dysplasia --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:pyle metaphyseal dysplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 syndrome d'alagille --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome d'alagille | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 une anomalie congénitale --- r_associated #0: 22 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=une anomalie congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=22 Marfan (maladie de) --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Marfan (maladie de) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 aplasie de la paroi abdominale --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=aplasie de la paroi abdominale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:autosomal dominant hypophosphatemic bone disease --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant hypophosphatemic bone disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:autosomal dominant ichthyosis --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:autosomal dominant ichthyosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:col1a1 associated connective tissue disorder --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:col1a1 associated connective tissue disorder | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:exomphalos --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:exomphalos | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:hereditary motor and sensory neuropathy type I --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary motor and sensory neuropathy type I | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:hereditary multiple ossifying ecchondromata --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary multiple ossifying ecchondromata | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:loeys-dietz syndrome --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:loeys-dietz syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:marfan's syndrome --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:marfan's syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:schnyder crystalline corneal dystrophy --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:schnyder crystalline corneal dystrophy | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 en:uv-sensitive syndrome --- r_associated #0: 21 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:uv-sensitive syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=21 Malformation congénitale --- r_associated #0: 20 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Malformation congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=20 syndrome --- r_associated #0: 20 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=20 Maladie de Marfan --- r_associated #0: 15 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Maladie de Marfan | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=15 Syndrome de Lynch --- r_associated #0: 15 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Syndrome de Lynch | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=15 démence (sémiologie) --- r_associated #0: 15 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=démence (sémiologie) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=15 en:tylose --- r_associated #0: 15 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:tylose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=15 malentendant (enfant) --- r_associated #0: 15 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malentendant (enfant) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=15 Bessel-Hagen (maladie de) --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Bessel-Hagen (maladie de) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 CONGÉNITALE --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=CONGÉNITALE | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 Gorlin (syndrome de) --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Gorlin (syndrome de) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 Hypertélorisme --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Hypertélorisme | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 MIGP (orientation) --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=MIGP (orientation) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 Malformation --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Malformation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 Neurofibromatose --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Neurofibromatose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 Tylosis --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Tylosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 absence d'empreintes digitales avec syndrome de milia congénital --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=absence d'empreintes digitales avec syndrome de milia congénital | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 angl. HNPCC --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=angl. HNPCC | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:Crouzon's disease --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Crouzon's disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:Crouzon?s disease --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Crouzon?s disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:LEOPARD syndrome --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:LEOPARD syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:Recklinghausen's disease --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:Recklinghausen's disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:abdominal wall aplasia --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:abdominal wall aplasia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:and sensorineural deafness --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:and sensorineural deafness | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:atypical nevus syndrome --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:atypical nevus syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:cacomorphosis --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:cacomorphosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:contractural arachnodactyly --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:contractural arachnodactyly | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:dysplastic nevus syndrome hereditary --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:dysplastic nevus syndrome hereditary | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:eds --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:eds | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:ehlers danlos syndrome --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:ehlers danlos syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:facial clefting syndrome --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:facial clefting syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:hyperkeratosis of nipple and areola --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hyperkeratosis of nipple and areola | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:hypoacousic child --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypoacousic child | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:hypospadias --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hypospadias | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:iris coloboma with ptosis --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:iris coloboma with ptosis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:microtia --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:microtia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:myopia --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:myopia | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:polysyndactyly syndrome --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:polysyndactyly syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:type I --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:type I | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:type VI --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:type VI | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:von recklinghausen's disease --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:von recklinghausen's disease | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 en:xanthine lithiasis --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:xanthine lithiasis | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 exostose du conduit auditif externe --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=exostose du conduit auditif externe | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 exostose ostéocartilagineuse --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=exostose ostéocartilagineuse | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 exostose sous-unguéale --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=exostose sous-unguéale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 exostosectomie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=exostosectomie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 goniome --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=goniome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 goniomètre --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=goniomètre | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonion --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonion | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonioscopie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonioscopie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 goniosynéchies --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=goniosynéchies | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 goniotomie endoscopique --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=goniotomie endoscopique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonochorisme --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonochorisme | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonococcie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonococcie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonocoque --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonocoque | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonocyte --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonocyte | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonocytome --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonocytome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonométrie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonométrie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonorrhée --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonorrhée | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonosome --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonosome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 gonosomique --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=gonosomique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hernie diaphragmatique --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hernie diaphragmatique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hyperkeratosis follicularis et parafollicularis in cutem penetrans de Kyrle --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperkeratosis follicularis et parafollicularis in cutem penetrans de Kyrle | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hyperkeratosis lenticularis perstans de Flegel --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperkeratosis lenticularis perstans de Flegel | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hyperkinésie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperkinésie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hyperkinésie volitionnelle --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperkinésie volitionnelle | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hyperlacrymie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperlacrymie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hyperlactacidémie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperlactacidémie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hyperlaxité articulaire familiale --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperlaxité articulaire familiale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hypertensinase --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hypertensinase | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hypertensine --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hypertensine | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hypertensinogène --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hypertensinogène | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hypertension --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hypertension | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hypertension abdominale --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hypertension abdominale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 hypertension artérielle --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hypertension artérielle | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 neuropathie sensitivomotrice héréditaire forme I --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=neuropathie sensitivomotrice héréditaire forme I | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 nystagmus --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nystagmus | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 nystagmus héréditaire vertical --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nystagmus héréditaire vertical | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 nystagmus lié au sexe --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nystagmus lié au sexe | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 nystagmus myoclonies --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nystagmus myoclonies | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 omphalocèle --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=omphalocèle | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 paraplégie spastique dans la syphilis congénitale --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=paraplégie spastique dans la syphilis congénitale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 reclassement professionnel --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=reclassement professionnel | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 steatocystoma multiplex --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=steatocystoma multiplex | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 syndrome de Feingold --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de Feingold | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 syndrome de Nathalie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de Nathalie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 syndrome de Pitt-Hopkins --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de Pitt-Hopkins | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 ty (élément) --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=ty (élément) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 télécardiographie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télécardiographie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 télécardiophone --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télécardiophone | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 téléclitoridie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=téléclitoridie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 télécobalt --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télécobalt | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 télécobalt-thérapie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télécobalt-thérapie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 téléconsultation --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=téléconsultation | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 télécrâne --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télécrâne | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 télécæsiothérapie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télécæsiothérapie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 télédermatologie --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télédermatologie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 télédiastole --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télédiastole | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 télédétection --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=télédétection | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 von Recklinghausen (maladie de) --- r_associated #0: 10 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=von Recklinghausen (maladie de) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=10 Alagille (syndrome d') --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Alagille (syndrome d') | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 Onsager (relation d') --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Onsager (relation d') | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 Stokvis-Talma (syndrome de) --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=Stokvis-Talma (syndrome de) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 albinisme cutanéo-oculaire --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=albinisme cutanéo-oculaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 démence d'Alzheimer --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=démence d'Alzheimer | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 hyperkératose talonnière fissurée --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperkératose talonnière fissurée | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 hyperleucocytose --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperleucocytose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 hyperlipémie --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=hyperlipémie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 lynestrénol --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=lynestrénol | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 lyo-enzyme --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=lyo-enzyme | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 lyoglycogène --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=lyoglycogène | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malf ormation dysraphique --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malf ormation dysraphique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation kystique adénomatoïde du poumon | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malformation luxante de la hanche --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation luxante de la hanche | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malformation mamelonnaire --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation mamelonnaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malformation mammaire --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation mammaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malformation ombilicale --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation ombilicale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malformation utérine --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation utérine | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malformation vaginale --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation vaginale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformation vasculaire cérébrale du nourrisson | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=malformations de la charnière occipitocervicale | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 nystagmus (zone de moindre) --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nystagmus (zone de moindre) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 nævique irien (syndrome) --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nævique irien (syndrome) | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 nævus dysplasique héréditaire --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nævus dysplasique héréditaire | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 nævus eccrine --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nævus eccrine | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 nævus elasticus --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nævus elasticus | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 nævus élastique en tumeurs disséminées --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nævus élastique en tumeurs disséminées | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 nævus épidermique --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=nævus épidermique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 onychodysplasie --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=onychodysplasie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 onychogryphose --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=onychogryphose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 onycholyse --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=onycholyse | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 onycholyse candidosique --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=onycholyse candidosique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 onycholyse semi-lunaire partielle --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=onycholyse semi-lunaire partielle | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 onychomadèse --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=onychomadèse | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 onychomatricome --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=onychomatricome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 syndrome d'Ehlers-Danlos --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome d'Ehlers-Danlos | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 syndrome de Stickler --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome de Stickler | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 syndrome lymphoprolifératif avec autoimmunité --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=syndrome lymphoprolifératif avec autoimmunité | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthoastrocytome pléomorphe | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthochromie --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthochromie | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthochromie caroténique --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthochromie caroténique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthoerythrodermia perstans --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthoerythrodermia perstans | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthogranulome juvénile --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthogranulome juvénile | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthogranulome nécrobiotique | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthogranulome palpébral --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthogranulome palpébral | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthohistiocytome --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthohistiocytome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthoma disseminatum --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthoma disseminatum | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5 xanthomatose --- r_associated #0: 5 --> en:crouzon syndrome with acanthosis nigricans (disorder) n1=xanthomatose | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=5