Familial medullary thyroid carcinoma
GPTKB entity
Statements (27)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
hereditary cancer syndrome |
| gptkbp:alsoKnownAs |
gptkb:FMTC
|
| gptkbp:associatedWith |
gptkb:multiple_endocrine_neoplasia_type_2
RET gene mutation |
| gptkbp:canMetastasizeTo |
gptkb:bone
lungs liver lymph nodes |
| gptkbp:diagnosedBy |
genetic testing
calcitonin measurement |
| gptkbp:firstDescribed |
1960s
|
| https://www.w3.org/2000/01/rdf-schema#label |
Familial medullary thyroid carcinoma
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:marking |
gptkb:calcitonin
carcinoembryonic antigen (CEA) |
| gptkbp:prevalence |
rare
|
| gptkbp:primarySite |
thyroid gland
|
| gptkbp:prognosis |
variable
|
| gptkbp:riskFactor |
family history of medullary thyroid carcinoma
|
| gptkbp:subspecies |
gptkb:medullary_thyroid_carcinoma
|
| gptkbp:symptom |
diarrhea
flushing neck mass |
| gptkbp:treatment |
thyroidectomy
|
| gptkbp:bfsParent |
gptkb:Medullary_thyroid_cancer
|
| gptkbp:bfsLayer |
5
|