eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | c syndrome |
| Comorbidity | C0035309|retinal disorders |
| Sentences | 1 |
| PubMedID- 20723134 | Defects in the gene encoding fh are associated with human diseases like severe kidney and retinal disorders in the form of atypical haemolytic uremic syndrome (ahus), membranoproliferative glomerulonephritis ii (mpgn ii) or age-related macular degeneration (amd). |
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