| Symbol
| MEN1
|
| Location
| 11q13.2
|
| Name
|
endocrine neoplasia, multiple, type 1 |
| Other name(s)
|
endocrine adenomatosis, multiple
. Wermer syndrome (MEN1 defect) |
| Corresponding gene
|
MEN1
|
| related resource
| Multiple Endocrine Neoplasia type 1 Mutation Database
|
| Other symbol(s)
| MEA1
|
| Main clinical features
|
hyperparathyroidism, gastrinoma somatotrophinoma, prolactinoma, including somatic mutations in sporadic neuroendocrine and pancreatic tumors, and carcinoid tumors of lungs and in fore foregut neoplasms, excluding the sporadic hyperplastic or neoplastic lesions of the adrenal cortex |
| Genetic determination
| autosomal dominant |
| Related entries
| Zollinger-Ellison syndrome and lipoma and angiofibroma sporadic
|
| Function/system disorder
| endocrinology |
| Type
| disease
|