Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 6p22 microdeletion syndrome is a newly described syndrome associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations. Disease data Classification Malformation syndrome Synonyms Del(6)(p22) Del(6)(p22) Monosomia 6p22 Monosomy 6p22 ORPHA code 251046 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