flat capital femoral epiphysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal flattening of the proximal epiphysis of the femur. (Human Phenotype Ontology, HP_0003370)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003370
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8 genes associated with the flat capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACAN aggrecan
COL2A1 collagen, type II, alpha 1
GNPTG N-acetylglucosamine-1-phosphate transferase, gamma subunit
KIF22 kinesin family member 22
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC39A13 solute carrier family 39 (zinc transporter), member 13
TBX4 T-box 4
TRPS1 trichorhinophalangeal syndrome I