Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000991276 | SCV001142658 | likely pathogenic | MEHMO syndrome | 2017-12-19 | criteria provided, single submitter | clinical testing |