loading...| Preferred Name | multiple endocrine neoplasia type 1 | |
| Synonyms |
MEA 1 endocrine adenomatosis multiple multiple endocrine neoplasia, type 1 MEN1 somatic mutations endocrine adenomatosis, multiple multiple endocrine adenomatosis Wermer's syndrome multiple endocrine adenomatosis, type I multiple endocrine neoplasia caused by mutation in MEN1 multiple endocrine neoplasia, type I multiple endocrine adenomatosis type 1 MEA type 1 MEA type I men 1 multiple endocrine neoplasia type I MEN1 syndrome MEN1 multiple endocrine neoplasia 1 men type I multiple endocrine neoplasia type 1 Wermer syndrome multiple endocrine adenomatosis type I men type 1 MEN1 multiple endocrine neoplasia multiple endocrine neoplasia type 1 syndrome |
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| Definitions |
Multiple endocrine neoplasia Type 1 (MEN1) is a frequent form of MEN, a rare inherited cancer syndrome, characterized by the development of neuroendocrine tumors of the parathyroid, pancreas, and anterior pituitary gland, and less commonly the adrenal cortical gland, with other non-endocrine tumors in some patients. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0007540 |
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| altLabel |
MEA 1 endocrine adenomatosis multiple multiple endocrine neoplasia, type 1 MEN1 somatic mutations endocrine adenomatosis, multiple multiple endocrine adenomatosis Wermer's syndrome multiple endocrine adenomatosis, type I multiple endocrine neoplasia caused by mutation in MEN1 multiple endocrine neoplasia, type I multiple endocrine adenomatosis type 1 MEA type 1 MEA type I men 1 multiple endocrine neoplasia type I MEN1 syndrome MEN1 multiple endocrine neoplasia 1 men type I multiple endocrine neoplasia type 1 Wermer syndrome multiple endocrine adenomatosis type I men type 1 MEN1 multiple endocrine neoplasia multiple endocrine neoplasia type 1 syndrome |
|
| definition |
Multiple endocrine neoplasia Type 1 (MEN1) is a frequent form of MEN, a rare inherited cancer syndrome, characterized by the development of neuroendocrine tumors of the parathyroid, pancreas, and anterior pituitary gland, and less commonly the adrenal cortical gland, with other non-endocrine tumors in some patients. |
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| has_broad_synonym |
multiple endocrine adenomatosis |
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| has_exact_synonym |
Wermer's syndrome multiple endocrine adenomatosis, type I multiple endocrine neoplasia caused by mutation in MEN1 multiple endocrine neoplasia, type I multiple endocrine adenomatosis type 1 MEA type 1 MEA type I men 1 multiple endocrine neoplasia type I MEN1 syndrome MEN1 multiple endocrine neoplasia 1 men type I multiple endocrine neoplasia type 1 Wermer syndrome multiple endocrine adenomatosis type I men type 1 MEN1 multiple endocrine neoplasia multiple endocrine neoplasia type 1 syndrome |
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| has_related_synonym |
MEA 1 endocrine adenomatosis multiple multiple endocrine neoplasia, type 1 MEN1 somatic mutations endocrine adenomatosis, multiple |
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| IAO_0000233 | ||
| label |
multiple endocrine neoplasia type 1 |
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| prefixIRI |
MONDO:0007540 |
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| prefLabel |
multiple endocrine neoplasia type 1 |
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| seeAlso |
https://rarediseases.info.nih.gov/diseases/3829/multiple-endocrine-neoplasia-type-1 |
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| textual definition |
Multiple endocrine neoplasia Type 1 (MEN1) is a frequent form of MEN, a rare inherited cancer syndrome, characterized by the development of neuroendocrine tumors of the parathyroid, pancreas, and anterior pituitary gland, and less commonly the adrenal cortical gland, with other non-endocrine tumors in some patients. |
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| subClassOf |
http://purl.obolibrary.org/obo/MONDO_0018538 http://purl.obolibrary.org/obo/MONDO_0017169 http://purl.obolibrary.org/obo/MONDO_0000426 |