Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Laboratory of Prof. |
RCV000225059 | SCV000281979 | pathogenic | Autosomal dominant nonsyndromic hearing loss 22 | 2016-02-16 | no assertion criteria provided | research | Childhood onset, moderate-profound HL |