Chondrosarcoma Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A slowly growing malignant neoplasm derived from cartilage cells, occurring most frequently in pelvic bones or near the ends of long bones, in middle-aged and old people. Most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion or in patients with ENCHONDROMATOSIS. (Stedman, 25th ed)|A malignant mesenchymal tumor arising from cartilage-forming tissues involving the bones. It affects middle-aged to elderly adults, and the pelvic bones, ribs, shoulder girdle, and long bones are the most common sites of involvement. Most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion. (Experimental Factor Ontology, EFO_0000333)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D002813
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Genes

2 genes/proteins associated with the disease Chondrosarcoma from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
EXT1 exostosin glycosyltransferase 1 2.88009
COL2A1 collagen, type II, alpha 1 2.88009