Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000513186 | SCV000608374 | pathogenic | Congenital adrenal hypoplasia, X-linked | 2017-09-20 | criteria provided, single submitter | clinical testing |