Source:http://linkedlifedata.com/resource/lhgdn/association:39947
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
The pathogenesis of the retinal dots and flecks in Alport syndrome is independent of CFH-dependent mechanisms and, like other clinical features, may depend on the nature of the underlying COL4A5 mutations.
|
| lhgdn:mesh_code |
D009394
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |