Isolated congenital hypogonadotropic hypogonadism

Orpha code: 238666OMIM code:

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
-

No additional description.

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