Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja 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 Klasyfikacja Malformation syndrome Synonimy 46,XX/46,XY chimerism Chimeryzm 46,XX/46,XY Kod ORPHA 199310 Kod OMIM - Kod ICD10 Q99.0 Kod ICD11 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