partial duplication of the phalanx of hand Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A partial duplication, depending on severity leading to a broad or bifid appearance, affecting one or more of the phalanges of the hand. As opposed to a complete duplication there is still a variable degree of fusion between the duplicated bones. (Human Phenotype Ontology, HP_0009999)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009999
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Genes

9 genes associated with the partial duplication of the 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
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
KIF7 kinesin family member 7
RPS19 ribosomal protein S19
SALL1 spalt-like transcription factor 1
TBX5 T-box 5
TWIST1 twist family bHLH transcription factor 1