| Dataset | CTD Gene-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://ctdbase.org/detail.go?type=disease&acc=MESH:D010040 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Otosclerosis from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| OTSC1 | otosclerosis 1 | 2.88009 |
