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| Term | familial male-limited precocious puberty | ID (Ontology) | DOID:0111545 (Human Disease) | |||||||||
| 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. | |||||||||||
| Also Known As | "familial gonadotropin-independent male-limited sexual precocity" ; "FMPP" ; "male-limited precocious puberty" (for all, see Synonyms field below) | |||||||||||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ disease of anatomical entity | |__endocrine system disease____| familial male-limited precocious puberty 1 rec. |
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autosomal dominant disease endocrine system disease |
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GARD:4475 MESH:C536961 MESH:D011629 MIM:176410 ORDO:3000 SNOMEDCT_US_2023_03_01:237818003 UMLS_CUI:C0342549 UMLS_CUI:C1504412 |
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