eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | usher syndrome type 3 |
| Comorbidity | C0271097|usher syndrome |
| Sentences | 1 |
| PubMedID- 22131869 | Rp shows no ethnic specificity, but rp caused by mutations in particular genes may be more frequent in certain isolated or consanguineous populations (such as the ush3 gene associated with type iii usher syndrome, normally rare, but more common among finns and ashkenazi jews). |
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