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Metadata
ID DOID:0111545
Name familial male-limited precocious puberty
Definition An endocrine system disease characterized by onset in early childhood of accelerated growth, early development of secondary sexual characteristics, and reduced adult height in males only that has_material_basis_in heterozygous mutation in the LHCGR gene on chromosome 2p16.3.
https://ghr.nlm.nih.gov/condition/familial-male-limited-precocious-puberty, https://www.ncbi.nlm.nih.gov/pubmed/7692306
Xrefs

GARD:4475

MESH:C536961

MESH:D011629

OMIM:176410

ORDO:3000

SNOMEDCT_US_2023_03_01:237818003

UMLS_CUI:C0342549

UMLS_CUI:C1504412

Subsets

DO_rare_slim

Synonyms

familial gonadotropin-independent male-limited sexual precocity [EXACT]

FMPP [EXACT]

male-limited precocious puberty [EXACT]

testotoxicosis [EXACT]

Parent Relationships

is_a endocrine system disease

is_a autosomal dominant disease

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