abnormality of the temporal bone Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of the temporal bone of the skull, which is situated at the sides and base of the skull roughly underlying the region of the face known as the temple. (Human Phenotype Ontology, HP_0009911)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009911
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Genes

2 genes associated with the abnormality of the temporal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GDF3 growth differentiation factor 3
GDF6 growth differentiation factor 6