irregular tarsal ossification Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Defective ossification in an irregular pattern of the seven bones of the foot comprising the calcaneus, talus, cuboid, navicular, and the cuneiform bones. (Human Phenotype Ontology, HP_0008134)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008134
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Genes

1 genes associated with the irregular tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3