| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A monogenic disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss. (Human Disease Ontology, DOID_10983) |
| External Link | http://www.omim.org/entry/301050 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the alport syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| COL4A5 | collagen, type IV, alpha 5 |
