Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare, sex chromosome disorder of sex development characterized by the two different haploid sets of maternal and paternal chromosomes and variable phenotype - from normal male or female genitalia, to different degrees of ambiguous genitalia, and often infertility. Also, in the cases of monochorionic dizygotic twins, it can be confined to blood of both twins. Disease data Classification Malformation syndrome Synonyms 46,XX/46,XY chimerism Chimeryzm 46,XX/46,XY ORPHA code 199310 OMIM code - ICD10 code Q99.0 ICD11 code LD56 *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