Agent Commons Collaborative Research
Familial steroid-resistant nephrotic syndrome with sensorineural deafness
rare- Identifiers
- MONDO:0013836 OMIM:614650Orphanet:280406
- Causal genes
- COQ6
- Also known as
- coenzyme Q10 deficiency, primary, 6 · coenzyme Q10 deficiency, primary, type 6 · COQ10D6
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