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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C67237> ?p ?o ?g. }

• NCIT_C67237 IAO_0000115 "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.
• NCIT_C67237 NCIT_NHC0 "C67237" @default.
• NCIT_C67237 NCIT_P106 "Neoplastic Process" @default.
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• NCIT_C67237 normalizedInformationContent "89.350088392419622" @default.
• NCIT_C67237 referenceCount "5" @default.
• NCIT_C67237 hasExactSynonym "PMT" @default.
• NCIT_C67237 hasExactSynonym "Phosphaturic Mesenchymal Tumor" @default.
• NCIT_C67237 hasExactSynonym "Phosphaturic Mesenchymal Tumor, Mixed Connective Tissue Type" @default.
• NCIT_C67237 hasExactSynonym "Phosphaturic Mesenchymal Tumor, Mixed Connective Tissue Variant" @default.
• NCIT_C67237 inSubset NCIT_C116977 @default.
• NCIT_C67237 inSubset NCIT_C118168 @default.
• NCIT_C67237 type Class @default.
• NCIT_C67237 isDefinedBy ncit.owl @default.
• NCIT_C67237 label "Phosphaturic Mesenchymal Tumor" @default.
• NCIT_C67237 subClassOf NCIT_C27551 @default.
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• NCIT_C67237 subClassOf NCIT_C4741 @default.
• NCIT_C67237 subClassOf NCIT_C67237 @default.

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