eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | bardet-biedl syndrome |
| Comorbidity | C0022658|renal disease |
| Sentences | 2 |
| PubMedID- 22190896 | Mutations in sdccag8/nphp10 cause bardet-biedl syndrome and are associated with penetrant renal disease and absent polydactyly. |
| PubMedID- 25664275 | bardet-biedl syndrome: a rare cause of end stage renal disease. |
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