brachytelomesophalangy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Disproportionately short middle and distal phalanges compared to the hand/foot. (Human Phenotype Ontology, HP_0005872)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005872
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Genes

1 genes associated with the brachytelomesophalangy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TRPV4 transient receptor potential cation channel, subfamily V, member 4