| Dataset | GWASdb SNP-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Formation of spongy bone in the labyrinth capsule which can progress toward the STAPES (stapedial fixation) or anteriorly toward the COCHLEA leading to conductive, sensorineural, or mixed HEARING LOSS. Several genes are associated with familial otosclerosis with varied clinical signs. (Experimental Factor Ontology, EFO_0004213) |
| External Link | http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:12185 |
| Similar Terms | |
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5 genes associated with the disease otosclerosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
