Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare, inherited disorder characterized by widespread calcifications of basal ganglia and cortex, developmental delay, small stature, retinopathy and microcephaly. The absence of progressive deterioration of the neurological functions is characteristic of the disease. Disease data Classification Disease ORPHA code 178506 OMIM code 613658 ICD10 code G93.8 ICD11 code LD20.4 *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