loading...| Preferred Name | multiple endocrine neoplasia type 1 | |
| Synonyms |
Wermer syndrome Wermer's syndrome MEN type I |
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| Definitions |
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]. |
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| ID |
http://purl.obolibrary.org/obo/DOID_10017 |
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| Obsolete |
true |
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| comment |
OMIM mapping confirmed by DO. [SN]. |
|
| alternative label |
Wermer syndrome Wermer's syndrome MEN type I |
|
| database_cross_reference |
ICD9CM:258.01 OMIM:131100 MESH:D018761 UMLS_CUI:C0025267 SNOMEDCT_US_2023_03_01:30664006 ICD10CM:E31.21 GARD:3829 NCI:C3225 ORDO:652 |
|
| definition |
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 exact synonym |
Wermer syndrome Wermer's syndrome MEN type I |
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| has material basis in | ||
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:10017 |
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| in_subset | ||
| label |
multiple endocrine neoplasia type 1 |
|
| notation |
DOID:10017 |
|
| note |
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]. |
|
| owl:deprecated |
true |
|
| preferred label |
multiple endocrine neoplasia type 1 |
|
| prefLabel |
multiple endocrine neoplasia type 1 |
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| subClassOf |