| 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 |
| Similar Terms | |
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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.
