Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
OMIM | RCV000488562 | SCV000029566 | pathogenic | Pulmonary hypertension, primary, 1 | 2000-09-01 | no assertion criteria provided | literature only | |
Rare Disease Genomics Group, |
RCV000488562 | SCV000576164 | pathogenic | Pulmonary hypertension, primary, 1 | no assertion criteria provided | literature only |