Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
OMIM | RCV002279942 | SCV000035515 | pathogenic | Neuropathy, congenital hypomyelinating, 2 | 2003-09-01 | no assertion criteria provided | literature only | |
Inherited Neuropathy Consortium | RCV000789489 | SCV000928845 | uncertain significance | Charcot-Marie-Tooth disease | no assertion criteria provided | literature only |