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- B1b006054e15c2f1646592cad86fb812a hasDbXref "Orphanet:143" @default.
- B1b006054e15c2f1646592cad86fb812a hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B1b006054e15c2f1646592cad86fb812a type Axiom @default.
- B1b006054e15c2f1646592cad86fb812a annotatedProperty IAO_0000115 @default.
- B1b006054e15c2f1646592cad86fb812a annotatedSource MONDO_0012004 @default.
- B1b006054e15c2f1646592cad86fb812a annotatedTarget "A very rare, slow-growing, clinically serious endocrine tumor that generally develops in mid-adulthood. PRTC presents as a palpable painless mass in the neck and causes severe hypercalcemia and related symptoms, non-specific gastrointestinal manifestations, as well as renal and bone complications related to primary hyperparathyroidism (nephrolithiasis, impaired renal function, osteoporosis, bone pain, and pathologic fractures, etc.). Some PRTCs are however non-functioning tumors." @default.