short middle phalanx of toe Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Developmental hypoplasia (shortening) of middle phalanx of toe. (Human Phenotype Ontology, HP_0003795)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003795
Similar Terms
Downloads & Tools

Genes

5 genes associated with the short middle phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
HOXD13 homeobox D13
TRPV4 transient receptor potential cation channel, subfamily V, member 4