abnormality of the proximal phalanx of the 5th finger Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of the proximal phalanx of the little (5th) finger. (Human Phenotype Ontology, HP_0009150)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009150
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
NOG noggin