alport syndrome Gene Set
| Dataset |
GAD Gene-Disease Associations
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| Category |
disease or phenotype associations
|
| Type |
disease |
| Description |
A monogenic disease that is characterized by glomerulonephritis, endstage kidney disease, and hearing loss. (Human Disease Ontology, DOID_10983)
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| Similar Terms |
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| Downloads & Tools |
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Genes
1 genes associated with the disease alport syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
| Symbol |
Name |
|
COL4A5
|
collagen, type IV, alpha 5
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