Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition An extremely rare autosomal dominant developmental defect of the eye described in several members of one family that is characterized by the association of moderate intellectual disability with aniridia, lens dislocation, optic nerve hypoplasia and cataracts. There have been no further descriptions in the literature since 1974. Disease data Classification Malformation syndrome Synonyms Walker-Dyson syndrome Zespół Walkera i Dysona ORPHA code 1068 OMIM code - ICD10 code Q13.1 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl