Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare, genetic pituitary hormone deficiency characterized by gonadotropin (Gn) deficiency with low sex steroid levels associated with low levels of follicle stimulating hormone (FSH) and luteinizing hormone (LH). This disorder may be associated with a normal (normosmic) or impaired sense of smell (Kallmann syndrome). Disease data Klasyfikacja Disease Synonimy Gonadotropic deficiency Isolated congenital gonadotropin deficiency Isolated gonadotropin-releasing hormone deficiency Gonadotropic deficiency Isolated congenital gonadotropin deficiency Isolated gonadotropin-releasing hormone deficiency Kod ORPHA 238666 Kod OMIM - Kod ICD10 E23.0 Kod ICD11 - *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