Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Medical Molecular Genetics Department, |
RCV001291626 | SCV001480043 | pathogenic | Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive | 2021-02-13 | criteria provided, single submitter | research |