Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 20p12.3 microdeletion syndrome is a recently described syndrome characterized by Wolff-Parkinson-White syndrome (see this term), variable developmental delay and facial dysmorphism. Disease data Classification Malformation syndrome Synonyms Del(20)(p12.3) Del(20)(p12.3) Monosomia 20p12.3 Monosomy 20p12.3 ORPHA code 261295 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