'en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome'
(id=9102793 ; fe=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=1978 creation date=2017-10-29 touchdate=2024-09-20 01:22:50.000)

≈ 65 relations sortantes en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 27 / 1 -> syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=syndrome | rel=r_associated | relid=0 | w=27 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:acrorenal mandibular syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:adducted thumbs and arthrogryposis syndrome christian type n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:anauxetic dysplasia n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:arthrogryposis renal dysfunction cholestasis syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:arthrogryposis renal dysfunction cholestasis syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:autosomal recessive spastic paraplegia type 39 n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:autosomal recessive spastic paraplegia type 39 | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:bamforth syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:bestrophinopathy, autosomal recessive n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:bestrophinopathy, autosomal recessive | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:braddock syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:brain calcification rajab type n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:cervical hypertrichosis and peripheral neuropathy syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:congenital analbuminemia n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:congenital cataract with ataxia and deafness syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:congenital disorder of glycosylation type 1h n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:congenital disorder of glycosylation type 1h | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:congenital disorder of glycosylation type 2e n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:congenital disorder of glycosylation type 2e | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:congenital disorder of glycosylation type id n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:congenital disorder of glycosylation type id | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:congenital disorder of glycosylation type ie n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:congenital disorder of glycosylation type ie | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:congenital disorder of glycosylation, type if n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:congenital disorder of glycosylation, type if | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:cooper jabs syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:craniofacial ulnar renal syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:craniofacial ulnar renal syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:cutaneous photosensitivity and lethal colitis syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:deafness and myopia syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:diaphanospondylodysostosis n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:didymosis aplasticosebacea n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:didymosis aplasticosebacea | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:distal monosomy 10q syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:distal monosomy 10q syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:double uterus, hemivagina, renal agenesis syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:double uterus, hemivagina, renal agenesis syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:dyschondrosteosis and nephritis syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:ectodermal dysplasia with blindness syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:familial median cleft of upper and lower lip n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:fountain syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:generalized peeling skin syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:hall riggs syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:heart defects limb shortening n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:hypomandibular faciocranial dysostosis n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:insulin growth factor i deficiency n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:kallman syndrome with heart disease n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:late-onset junctional epidermolysis bullosa n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:lethal larsen-like syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:manouvrier syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:microcephaly albinism digital anomalies syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:moyamoya disease with early onset achalasia n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:najjar syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:oculocutaneous albinism type 6 n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:oculocutaneous albinism type 6 | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:pelviscapular dysplasia n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:pili torti onychodysplasia syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:renal dysplasia - limb defects syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:robinow-like syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:split-hand/foot malformation 3 n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:spondyloepiphyseal dysplasia tarda kohn type n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:thoraco-abdominal enteric duplication n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:thoraco-abdominal enteric duplication | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:timothy syndrome type 2 n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:yemenite deaf-blind hypopigmentation syndrome n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome -- r_associated #0: 20 / 0.741 -> en:zellweger-like syndrome without peroxisomal anomaly n1=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | n2=en:zellweger-like syndrome without peroxisomal anomaly | rel=r_associated | relid=0 | w=20

≈ 65 relations entrantes en:oculocutaneous albinism type 6 --- r_associated #0: 41 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:oculocutaneous albinism type 6 | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=41 en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 40 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=40 en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 40 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=40 en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 36 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=36 en:autosomal recessive spastic paraplegia type 39 --- r_associated #0: 35 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:autosomal recessive spastic paraplegia type 39 | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=35 en:braddock syndrome --- r_associated #0: 35 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:braddock syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=35 en:congenital disorder of glycosylation type 2e --- r_associated #0: 35 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:congenital disorder of glycosylation type 2e | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=35 en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 35 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=35 en:late-onset junctional epidermolysis bullosa --- r_associated #0: 35 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:late-onset junctional epidermolysis bullosa | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=35 en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 35 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:microcephaly albinism digital anomalies syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=35 en:moyamoya disease with early onset achalasia --- r_associated #0: 35 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:moyamoya disease with early onset achalasia | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=35 en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 35 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=35 en:acrorenal mandibular syndrome --- r_associated #0: 34 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:acrorenal mandibular syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=34 en:bamforth syndrome --- r_associated #0: 34 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:bamforth syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=34 en:congenital analbuminemia --- r_associated #0: 34 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:congenital analbuminemia | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=34 en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 32 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=32 en:brain calcification rajab type --- r_associated #0: 32 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:brain calcification rajab type | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=32 en:congenital disorder of glycosylation type 1h --- r_associated #0: 32 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:congenital disorder of glycosylation type 1h | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=32 en:congenital disorder of glycosylation type ie --- r_associated #0: 32 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:congenital disorder of glycosylation type ie | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=32 en:lethal larsen-like syndrome --- r_associated #0: 32 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:lethal larsen-like syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=32 en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 32 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=32 en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:diaphanospondylodysostosis --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:diaphanospondylodysostosis | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:generalized peeling skin syndrome --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:generalized peeling skin syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:manouvrier syndrome --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:manouvrier syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:najjar syndrome --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:najjar syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:primary immunodeficiency syndrome due to p14 deficiency --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:renal dysplasia - limb defects syndrome --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:renal dysplasia - limb defects syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:timothy syndrome type 2 --- r_associated #0: 31 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:timothy syndrome type 2 | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=31 en:craniofacial ulnar renal syndrome --- r_associated #0: 30 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:craniofacial ulnar renal syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=30 en:double uterus, hemivagina, renal agenesis syndrome --- r_associated #0: 30 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:double uterus, hemivagina, renal agenesis syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=30 en:fountain syndrome --- r_associated #0: 30 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:fountain syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=30 en:robinow-like syndrome --- r_associated #0: 30 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:robinow-like syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=30 en:split-hand/foot malformation 3 --- r_associated #0: 30 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:split-hand/foot malformation 3 | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=30 en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 29 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=29 en:congenital disorder of glycosylation type id --- r_associated #0: 29 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:congenital disorder of glycosylation type id | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=29 en:didymosis aplasticosebacea --- r_associated #0: 29 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:didymosis aplasticosebacea | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=29 en:distal monosomy 10q syndrome --- r_associated #0: 29 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:distal monosomy 10q syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=29 en:insulin growth factor i deficiency --- r_associated #0: 29 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:insulin growth factor i deficiency | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=29 en:congenital disorder of glycosylation, type if --- r_associated #0: 28 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:congenital disorder of glycosylation, type if | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=28 en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 28 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:dyschondrosteosis and nephritis syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=28 en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 28 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:ectodermal dysplasia with blindness syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=28 en:hall riggs syndrome --- r_associated #0: 28 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:hall riggs syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=28 en:heart defects limb shortening --- r_associated #0: 28 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:heart defects limb shortening | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=28 en:hypomandibular faciocranial dysostosis --- r_associated #0: 28 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:hypomandibular faciocranial dysostosis | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=28 en:pili torti onychodysplasia syndrome --- r_associated #0: 28 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:pili torti onychodysplasia syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=28 en:arthrogryposis renal dysfunction cholestasis syndrome --- r_associated #0: 27 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:arthrogryposis renal dysfunction cholestasis syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=27 en:cooper jabs syndrome --- r_associated #0: 27 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:cooper jabs syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=27 en:kallman syndrome with heart disease --- r_associated #0: 27 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:kallman syndrome with heart disease | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=27 en:thoraco-abdominal enteric duplication --- r_associated #0: 27 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:thoraco-abdominal enteric duplication | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=27 en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 27 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=27 en:anauxetic dysplasia --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:anauxetic dysplasia | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 en:bestrophinopathy, autosomal recessive --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:bestrophinopathy, autosomal recessive | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 en:deafness and myopia syndrome --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:deafness and myopia syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 en:familial median cleft of upper and lower lip --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:familial median cleft of upper and lower lip | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 en:pelviscapular dysplasia --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:pelviscapular dysplasia | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 en:zellweger-like syndrome without peroxisomal anomaly --- r_associated #0: 26 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=en:zellweger-like syndrome without peroxisomal anomaly | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=26 syndrome --- r_associated #0: 20 --> en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome n1=syndrome | n2=en:anophthalmia and megalocornea with cardiopathy and skeletal anomalies syndrome | rel=r_associated | relid=0 | w=20