MeSH Browser

MeSH Supplementary: Familial Testotoxicosis
Unique ID: C536961
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536961
Entry Term(s): Familial Gonadotrophin-Independent Sexual Precocity; Familial Male-Limited Precocious Puberty; Gonadotrophin-Independent Precocious Puberty; Precocious Pseudopuberty; Sexual precocity, familial, gonadotropin-independent; Testotoxicosis, Familial
Registry Number: 0
Heading Mapped to: *Puberty, Precocious
Frequency: 53
Note: Hereditary, GONADOTROPIN-independent, precocious puberty that occurs in boys before 4 years of age. It is associated with mutations in the LHCGR gene. OMIM: 176410
Date of Entry: 2010/08/25
Revision Date: 2016/08/01

Familial Testotoxicosis MeSH Supplementary Concept Data 2024