MeSH Browser

MeSH Supplementary: Idiopathic Hypogonadotropic Hypogonadism
Unique ID: C562785
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562785
Entry Term(s): HH7; Hypogonadotropic Hypogonadism 7 With Or Without Anosmia
Registry Number: 0
Heading Mapped to: *Hypogonadism
Frequency: 101
Note: A hereditary autosomal recessive type of hypogonadism characterized by absent or incomplete sexual maturation by age 18 and low levels of circulating GONADOTROPINS and TESTOSTERONE and no other abnormalities of the hypothalamic-pituitary axis. Nonreproductive phenotypes, such as ANOSMIA; CLEFT PALATE, and SENSORINEURAL HEARING LOSS may also occur. Mutations in the GNRHR gene (gonadotropin-releasing hormone receptor) have been identified for HH7. OMIM: 146110
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Idiopathic Hypogonadotropic Hypogonadism MeSH Supplementary Concept Data 2024