PedAM
Pediatric Disease Annotations & Medicines
| Disease | retinal disease |
| Phenotype | C0271097|usher syndrome |
| Sentences | 1 |
| PubMedID- 25649381 | When allelic heterogeneity was studied and compared with that reported in usher syndrome, the concept of ‘retinal disease-specific' ush2a alleles (ie, alleles associated with retinal degeneration and no hearing complaint in childhood) became apparent. |
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