Puberty, Precocious
Disease ID: disease_node_6420
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| Dbxref | GARD:4475, MESH:C536961, MESH:D011629, MIM:176410, ORDO:3000, SNOMEDCT_US_2023_03_01:237818003, UMLS_CUI:C0342549, UMLS_CUI:C1504412 |
|---|---|
| Subclassof | DOID_0050736, DOID_28 |
| Data Source | DOID, MESH |
| Synonyms | FMPP, familial gonadotropin-independent male-limited sexual precocity, male-limited precocious puberty, testotoxicosis |
| Mesh Id | D011629 |
| Mesh Label | Puberty, Precocious |
| Mesh Subclassof | D006058 |
| Doid Label | familial male-limited precocious puberty |
| Doid 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. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_6420 |
| Doid Id | DOID_0111545 |
| Label | Puberty, Precocious |
- Outgoing r'ship
SUBCLASS_OFto/from Endocrine System Diseases(ID:disease_node_2920) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)