Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Génétique des Maladies du Développement, |
RCV000760231 | SCV000890062 | likely pathogenic | Syndromic X-linked intellectual disability Claes-Jensen type | 2017-03-16 | criteria provided, single submitter | clinical testing |