absent middle phalanx of 5th finger Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the middle phalanx of the little (5th) finger. (Human Phenotype Ontology, HP_0009162)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009162
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Genes

1 genes associated with the absent middle phalanx of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GJA1 gap junction protein, alpha 1, 43kDa