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Disease Ontology Browser
familial male-limited precocious puberty (DOID:0111545)
Alliance: disease page
Synonyms: familial gonadotropin-independent male-limited sexual precocity; FMPP; male-limited precocious puberty; testotoxicosis
Alt IDs: OMIM:176410, MESH:C536961, MESH:D011629, ORDO:3000, UMLS_CUI:C0342549, UMLS_CUI:C1504412
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory