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