Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
OMIM | RCV000012359 | SCV000032593 | pathogenic | Lissencephaly type 1 due to doublecortin gene mutation | 1998-01-09 | no assertion criteria provided | literature only | |
OMIM | RCV000012360 | SCV000032594 | pathogenic | Subcortical laminar heterotopia, X-linked | 1998-01-09 | no assertion criteria provided | literature only |