Statements (25)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
|
| gptkbp:alsoKnownAs |
gptkb:Multiple_Endocrine_Neoplasia_type_2
|
| gptkbp:associatedWith |
gptkb:pheochromocytoma
gptkb:medullary_thyroid_carcinoma parathyroid adenoma |
| gptkbp:diagnosedBy |
genetic testing
|
| gptkbp:firstDescribed |
gptkb:John_Sipple
|
| gptkbp:guidanceSystem |
gptkb:American_Thyroid_Association_guidelines
|
| https://www.w3.org/2000/01/rdf-schema#label |
MEN2
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:inheritsFrom |
autosomal dominant
|
| gptkbp:mutationAssociatedWith |
gptkb:RET_gene
|
| gptkbp:OMIM |
171400
|
| gptkbp:prevalence |
rare
|
| gptkbp:riskFactor |
family history of MEN2
|
| gptkbp:subspecies |
gptkb:Familial_medullary_thyroid_carcinoma
gptkb:MEN2A gptkb:MEN2B |
| gptkbp:symptom |
gptkb:hypercalcemia
hypertension thyroid nodule |
| gptkbp:treatment |
thyroidectomy
adrenalectomy |
| gptkbp:bfsParent |
gptkb:multiple_endocrine_neoplasia_type_2
|
| gptkbp:bfsLayer |
6
|