|
| General Information | |||
|---|---|---|---|
| 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) | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
||||||
autosomal genetic disease |__autosomal dominant disease__ disease of anatomical entity | |__endocrine system disease____| familial male-limited precocious puberty 1 rec. |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
autosomal dominant disease endocrine system disease |
||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
GARD:4475 MESH:C536961 MESH:D011629 MIM:176410 ORDO:3000 SNOMEDCT_US_2023_03_01:237818003 UMLS_CUI:C0342549 UMLS_CUI:C1504412 |
|||