familial male-limited precocious puberty

Summary

DOID:0111545 - familial male-limited precocious puberty

Disease Ontology 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.

Synonyms: familial gonadotropin-independent male-limited sexual precocity, FMPP, male-limited precocious puberty, testotoxicosis

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: lhcgr

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), endocrine system disease (is_a)