Carney Complex
Disease ID: disease_node_12272
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| Dbxref | GARD:1119, MESH:D056733, MIM:160980, MIM:605244, MIM:608837, NCI:C4705, ORDO:1359, SNOMEDCT_US_2023_03_01:733491005, UMLS_CUI:C0406810, UMLS_CUI:C1854540, UMLS_CUI:C2607929 |
|---|---|
| Subclassof | DOID_0050736, DOID_225 |
| Data Source | DOID, MESH |
| Synonyms | Carney Complex, Type 1, Carney Complex, Type 2, Carney Syndrome, Carney complex variant, LAMB Syndrome, NAME Syndrome |
| Mesh Id | D056733 |
| Mesh Label | Carney Complex |
| Mesh Subclassof | D000015, D009232, D012868, D006338 |
| Doid Label | Carney complex |
| Doid Description | A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_12272 |
| Doid Id | DOID_0050471 |
| Label | Carney Complex |
- Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)