Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000824885 | SCV000965795 | likely pathogenic | X-linked intellectual disability Cabezas type | 2014-01-01 | criteria provided, single submitter | clinical testing |