Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000995720 | SCV001150045 | pathogenic | Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome | 2018-05-09 | criteria provided, single submitter | clinical testing |