eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | glomerulonephritis |
| Comorbidity | C0155550|neural deafness |
| Sentences | 1 |
| PubMedID- 24988067 | Alport syndrome, historically referred to as hereditary glomerulonephritis with sensorineural deafness and anterior lenticonus, is a genetic disease of collagen alpha3alpha4alpha5(iv) resulting in renal failure. |
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