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- Bc1313fc69e6f398caac2af970564f5ac hasDbXref "NCIT:C3879" @default.
- Bc1313fc69e6f398caac2af970564f5ac type Axiom @default.
- Bc1313fc69e6f398caac2af970564f5ac annotatedProperty IAO_0000115 @default.
- Bc1313fc69e6f398caac2af970564f5ac annotatedSource MONDO_0015277 @default.
- Bc1313fc69e6f398caac2af970564f5ac annotatedTarget "A neuroendocrine carcinoma arising from the C-cells of the thyroid gland. It is closely associated with multiple endocrine neoplasia syndromes. Approximately 10% to 20% of medullary thyroid carcinomas are familial. Patients usually present with a thyroid nodule that is painless and firm. In the majority of cases nodal involvement is present at diagnosis. Surgery is the preferred treatment for both primary lesions and recurrences. This carcinoma is generally not very sensitive to radiation and almost unresponsive to chemotherapy." @default.