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DO Term : familial male-limited precocious puberty [DOID:0111545] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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,
  • OMIM:176410,
  • MESH:C536961,
  • MESH:D011629,
  • GARD:4475,
  • UMLS_CUI:C1504412,
  • UMLS_CUI:C0342549,
  • ORDO:3000,
  • male-limited precocious puberty,
  • 176410,
  • testotoxicosis,
  • SNOMEDCT_US_2023_03_01:237818003,
  • FMPP
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents