Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare genetic neurodevelopmental syndrome characterized by mild intellectual disability, developmental delay, dysmorphic facial features, growth- and feeding problems, hypotonia, epilepsy, behavioral problems and a variety of congenital abnormalities. Disease data Classification Malformation syndrome Synonyms SIN3A-related intellectual disability syndrome WITKOS SIN3A-related intellectual disability syndrome WITKOS ORPHA code 500163 OMIM code - ICD10 code - 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