Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Medical Biochemical Genetics, |
RCV000496176 | SCV000259182 | pathogenic | Congenital disorder of deglycosylation | 2016-01-07 | no assertion criteria provided | clinical testing |