Chondroma Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A cell type benign neoplasm that is a cartilaginous tumor encapsulated with a lobular growing pattern. (Human Disease Ontology, DOID_2602)
External Link https://www.disgenet.org/browser/0/1/0/C0936248
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Genes

13 genes associated with the disease Chondroma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACVR2A activin A receptor, type IIA
EXT1 exostosin glycosyltransferase 1
FGF23 fibroblast growth factor 23
FGFR1 fibroblast growth factor receptor 1
FN1 fibronectin 1
FPR2 formyl peptide receptor 2
HMGA2 high mobility group AT-hook 2
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial
RUNX2 runt-related transcription factor 2
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SLC29A2 solute carrier family 29 (equilibrative nucleoside transporter), member 2
TRIM27 tripartite motif containing 27