PedAM
Pediatric Disease Annotations & Medicines
| Disease | nephritis |
| Phenotype | C0155550|neural deafness |
| Sentences | 1 |
| PubMedID- 20884774 | Background and objectives: alport syndrome (as) is a predominantly x-linked hereditary nephritis associated with high-tone, sensorineural deafness and characteristic eye signs. |
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