Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000824879 | SCV000965788 | likely pathogenic | Syndromic X-linked intellectual disability Claes-Jensen type | 2015-01-01 | criteria provided, single submitter | clinical testing |