Congenital afibrinogenemia
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Congenital hypofibrinogenemia | C2584774 | FGA | Causal Pathogenic evidence from ClinVar | 1391954, 10602365, 10891444, 11460507, 12358944, 17295221, 18676163, 25427968 | ClinVar |
| FGB | Causal Pathogenic evidence from ClinVar | 10666208, 11460507, 11468164, 15070683, 17295221, 19404555, 25427968 | ClinVar | ||
| FGG | Causal Pathogenic evidence from ClinVar | 11460507, 17295221, 18676163, 25427968, 30349899 | ClinVar | ||
| ABCB11 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | 22120137 | - |