Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
NIHR Bioresource Rare Diseases, |
RCV000851817 | SCV000899801 | likely pathogenic | Hereditary factor IX deficiency disease | 2019-02-01 | criteria provided, single submitter | research | |
OMIM | RCV000010994 | SCV000031221 | pathogenic | Hereditary factor VIII deficiency disease | 1991-10-01 | no assertion criteria provided | literature only |