Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV001200912 | SCV001371833 | likely pathogenic | Autistic behavior; Delayed fine motor development; Moderate global developmental delay; Attention deficit hyperactivity disorder | 2018-11-03 | criteria provided, single submitter | clinical testing |