ICD-10: H53.433

Hirata disease obsolete peripheral dysostosis lacrimoauriculodentodigital syndrome 1 bradyopsia campomelic dysplasia obsolete tertiary syphilitic encephalitis Charcot-Marie-Tooth disease type 1 obsolete Majewski syndrome Ullrich congenital muscular dystrophy acrocapitofemoral dysplasia Aland Island eye disease anauxetic dysplasia 1 Baller-Gerold syndrome Bjornstad syndrome Borjeson-Forssman-Lehmann syndrome Athabaskan brainstem dysgenesis syndrome childhood electroclinical syndrome obsolete CLN3 disease ARC syndrome Meckel syndrome obsolete Opitz-GBBB syndrome iridogoniodysgenesis syndrome fibular hypoplasia and complex brachydactyly cerebral creatine deficiency syndrome 1 Stargardt disease developmental disorder of mental health Pearson syndrome astereognosia topographical agnosia acrofrontofacionasal dysostosis Warburg micro syndrome Van Maldergem syndrome Smith-McCort dysplasia pontocerebellar hypoplasia type 4 pontocerebellar hypoplasia type 10 Ohdo syndrome, SBBYS variant CEDNIK syndrome acromelic frontonasal dysostosis Galloway-Mowat syndrome 1 Parkinson's disease 15 orofaciodigital syndrome IV Joubert syndrome with orofaciodigital defect orofaciodigital syndrome VIII acrofacial dysostosis acrofacial dysostosis, Catania type acrofacial dysostosis, Patagonia type chromosome 15q11.2 deletion syndrome Cole-Carpenter syndrome Desbuquois dysplasia fibrochondrogenesis Goldberg-Shprintzen syndrome MEDNIK syndrome Kufor-Rakeb syndrome Char syndrome Ritscher-Schinzel syndrome hypertrichotic osteochondrodysplasia Cantu type Ritscher-Schinzel syndrome 2 lethal congenital contracture syndrome 4 cleft lip-palate-ectodermal dysplasia syndrome hypomyelinating leukodystrophy 10 Christianson syndrome Griscelli syndrome type 1 Leri-Weill dyschondrosteosis septooptic dysplasia patterned macular dystrophy 2