| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Absence of the inner ear due to a developmental defect. (Human Phenotype Ontology, HP_0011372) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0011372 |
| Similar Terms | |
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1 genes associated with the aplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FGF3 | fibroblast growth factor 3 |
