Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 16p13.11 microdeletion syndrome is a recently described syndrome characterized by developmental delay, microcephaly, epilepsy, short stature, facial dysmorphism and behavioral problems. Disease data Classification Malformation syndrome Synonyms Del(16)(p13.11) Del(16)(p13.11) Monosomia 16p13.11 Monosomy 16p13.11 ORPHA code 261236 OMIM code - ICD10 code Q93.5 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