PedAM
Pediatric Disease Annotations & Medicines
| Disease | ciliopathy |
| Phenotype | C0456909|blindness |
| Sentences | 1 |
| PubMedID- 22977115 | Ush2a and gpr98 have been found to be mutated in usher syndrome, a ciliopathy leading to deafness and blindness, and found to potentially interact in the extracellular gap (maerker et al. |
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