Multiple Endocrine Neoplasia Type 1
Disease ID: disease_node_9762
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| Dbxref | GARD:3829, ICD10CM:E31.21, ICD9CM:258.01, MESH:D018761, MIM:131100, NCI:C3225, ORDO:652, SNOMEDCT_US_2023_03_01:30664006, UMLS_CUI:C0025267 |
|---|---|
| Subclassof | DOID_0050736, DOID_3125 |
| Data Source | DOID, MESH |
| Synonyms | MEN type I, Wermer syndrome, Wermer's syndrome |
| Mesh Id | D018761 |
| Mesh Label | Multiple Endocrine Neoplasia Type 1 |
| Mesh Subclassof | D009377 |
| Doid Label | multiple endocrine neoplasia type 1 |
| Doid Description | A multiple endocrine neoplasia that has_material_basis_in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_9762 |
| Doid Id | DOID_10017 |
| Label | Multiple Endocrine Neoplasia Type 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Multiple Endocrine Neoplasia(ID:disease_node_5465) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)