duplication of the distal phalanx of hand Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	This term applies if one or more of the distal phalanges of the hand are either partially duplicated, depending on severity leading to a broad or bifid appearance of the phalanges, or completely duplicated. (Human Phenotype Ontology, HP_0009883)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0009883
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Genes

7 genes associated with the duplication of the distal phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
CANT1	calcium activated nucleotidase 1
FGFR2	fibroblast growth factor receptor 2
KIF7	kinesin family member 7
LMBR1	limb development membrane protein 1
ROR2	receptor tyrosine kinase-like orphan receptor 2
TWIST1	twist family bHLH transcription factor 1
WNT5A	wingless-type MMTV integration site family, member 5A