Multiple Endocrine Neoplasia type 2
GPTKB entity
Statements (31)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb: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
|
| gptkbp:ICD-10_code |
E31.2
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:mutationAssociatedWith |
gptkb:RET_gene
|
| gptkbp:OMIM |
171400
|
| gptkbp:onset |
childhood
adolescence adulthood |
| 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:Multiple_Endocrine_Neoplasia_type_1
gptkb:MEN2 gptkb:Pheochromocytoma gptkb:MEN2_syndrome |
| gptkbp:bfsLayer |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
Multiple Endocrine Neoplasia type 2
|