short middle phalanx of the 2nd finger Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hypoplasia (congenital reduction in size) of the middle phalanx of the second finger, also known as the index finger. (Human Phenotype Ontology, HP_0009577)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009577
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Genes

1 genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
RUNX2 runt-related transcription factor 2