multiple endocrine neoplasia syndrome type 2
GPTKB entity
Statements (26)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
|
| gptkbp:abbreviation |
gptkb:MEN2
|
| gptkbp:associatedWith |
gptkb:pheochromocytoma
gptkb:medullary_thyroid_carcinoma parathyroid adenoma |
| gptkbp:diagnosedBy |
genetic testing
|
| gptkbp:field |
endocrinology
|
| gptkbp:firstDescribed |
1961
|
| https://www.w3.org/2000/01/rdf-schema#label |
multiple endocrine neoplasia syndrome type 2
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:mutationAssociatedWith |
gptkb:RET_gene
|
| gptkbp:OMIM |
171400
|
| gptkbp:prevalence |
rare
|
| gptkbp:riskFactor |
family history of MEN2
|
| gptkbp:subspecies |
gptkb:MEN2A
gptkb:MEN2B gptkb:FMTC |
| gptkbp:symptom |
gptkb:hypercalcemia
hypertension thyroid nodule |
| gptkbp:treatment |
thyroidectomy
adrenalectomy |
| gptkbp:bfsParent |
gptkb:Mounjaro
gptkb:Trulicity gptkb:GLP-1_receptor_agonists |
| gptkbp:bfsLayer |
6
|