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- NCIT_C67235 IAO_0000115 "A paraneoplastic disorder affecting the skeletal system. It associated with one of four tumor types: phosphaturic mesenchymal tumor, mixed connective tissue type; osteoblastoma-like tumor; ossifying fibroma-like tumor or non-ossifying fibroma-like tumor. These neoplasms secrete fibroblast growth factor 23, which in addition to causing decreased renal phosphate reabsorption also affects the expression of 25-hydroxy-1-alpha-hydroxylase resulting in poor bone mineralization. Clinical signs include fractures, bone pain and muscle weakness. Once lesions are detected, prognosis is extremely favorable as resection most often results in cure." @default.
- NCIT_C67235 NCIT_NHC0 "C67235" @default.
- NCIT_C67235 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C67235 NCIT_P108 "Oncogenic Osteomalacia" @default.
- NCIT_C67235 NCIT_P207 "C1274103" @default.
- NCIT_C67235 NCIT_P366 "Oncogenic_Osteomalacia" @default.
- NCIT_C67235 NCIT_R100 NCIT_C12219 @default.
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- NCIT_C67235 NCIT_R108 NCIT_C77140 @default.
- NCIT_C67235 normalizedInformationContent "90.826665450122817" @default.
- NCIT_C67235 referenceCount "4" @default.
- NCIT_C67235 hasExactSynonym "Oncogenic Osteomalacia" @default.
- NCIT_C67235 type Class @default.
- NCIT_C67235 isDefinedBy ncit.owl @default.
- NCIT_C67235 label "Oncogenic Osteomalacia" @default.
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