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- B16b6d1704a9cbe94d76bdd8f11e08f30 NCIT_P378 "NCI" @default.
- B16b6d1704a9cbe94d76bdd8f11e08f30 type Axiom @default.
- B16b6d1704a9cbe94d76bdd8f11e08f30 annotatedProperty IAO_0000115 @default.
- B16b6d1704a9cbe94d76bdd8f11e08f30 annotatedSource NCIT_C67237 @default.
- B16b6d1704a9cbe94d76bdd8f11e08f30 annotatedTarget "An extremely rare, benign or malignant mesenchymal tumor arising from soft tissue or bone. It is a distinctive tumor, usually displaying the following morphologic characteristics: low cellularity, myxoid changes, presence of spindled cells and osteoclasts, hemangiopericytoma-like vessels, hemorrhage, and osteoid-like matrix. It is associated with the presence of a paraneoplastic syndrome called oncogenic osteomalacia. This syndrome usually precedes the appearance of the tumor, and it is characterized by phosphaturia, hypophosphatemia, normal serum calcium levels, and decreased levels of 1,25-dihydroxyvitamin D3. Patients present with bone and muscle pain, severe muscle weakness, fractures, gait disturbances, skeletal deformity, height loss, and slow growth. The metabolic disturbances improve or completely disappear after the complete resection of the tumor." @default.