Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
OMIM | RCV000018963 | SCV000039250 | pathogenic | Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome | 2007-12-27 | no assertion criteria provided | literature only | |
Gene |
RCV000018963 | SCV000055808 | not provided | Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome | no assertion provided | literature only |