| Metadata | |
|---|---|
| ID | DOID:10017 |
| Name | multiple endocrine neoplasia type 1 |
| 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. http://ghr.nlm.nih.gov/condition/multiple-endocrine-neoplasia, http://en.wikipedia.org/wiki/Multiple_endocrine_neoplasia_type_1, https://www.ncbi.nlm.nih.gov/pubmed/25509899, http://www.nlm.nih.gov/medlineplus/ency/article/000398.htm |
| Xrefs |
SNOMEDCT_US_2023_03_01:30664006 |
| Subsets |
DO_rare_slim NCIthesaurus |
| Synonyms |
MEN type I [EXACT] Wermer syndrome [EXACT] Wermer's syndrome [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |