"DOID:0111545"^^ . "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 LHCGR on chromosome 2p16.3."^^ . "OMIM:176410"^^ . . "UMLS_CUI:C0342549"^^ . "MESH:D011629"^^ . _:vb50945024 . _:vb50945024 . "SNOMEDCT_US_2021_09_01:237818003"^^ . "FMPP"@en . "UMLS_CUI:C1504412"^^ . _:vb50945024 . "MESH:C536961"^^ . "male-limited precocious puberty"@en . "disease_ontology"^^ . _:vb50945024 . "ORDO:3000"^^ . _:vb50945024 . . . "familial male-limited precocious puberty"^^ . "familial gonadotropin-independent male-limited sexual precocity"@en . "GARD:4475"^^ . "testotoxicosis"@en . .