Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare genetic disease characterized by mild intellectual disability, osteoporosis, delayed bone age, macrocephaly with wormian bones and frontal bossing, anomalies of fingers, nails, and teeth, thoracic deformities, hyperextensibility of joints, as well as congenital amaurosis and paraplegia. There have been no further descriptions in the literature since 1981. Disease data Classification Malformation syndrome Synonyms Heide syndrome Zespół Heidego ORPHA code 2787 OMIM code - ICD10 code Q87.5 ICD11 code LD24.KY *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