abnormality of the first metatarsal bone Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the first metatarsal bone. (Human Phenotype Ontology, HP_0010054)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010054
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6 genes associated with the abnormality of the first metatarsal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
ACVR1 activin A receptor, type I
CANT1 calcium activated nucleotidase 1
FGFR2 fibroblast growth factor receptor 2
HOXA13 homeobox A13
TWIST1 twist family bHLH transcription factor 1