| Hereditary Factor XI Deficiency |
C0015523 |
F11
|
Causal
Pathogenic evidence from ClinVar
|
1547342, 2052060, 2813350, 7669672, 7888672, 9401068, 9787168, 10027710, 10593931, 10606881, 11122101, 11127865, 11895778, 12716376, 12879434, 14508802, 14717969, 15026311, 15140127, 15180874, 15531455, 15634276, 15728123, 15749683, 15842381, 15946525, 15953011, 15968392, 16079124, 16519703, 16607084, 16787881, 16835901, 17229051, 17549289, 18005151, 18024374, 18312365, 18327400, 18446632, 18515884, 18758779, 18832909, 18839438, 19367158, 19652879, 20015217, 20398070, 20523169, 21192253, 21457405, 21649796, 21668437, 21718436, 21824284, 21999818, 22016685, 22159456, 22322133, 23305485, 23332144, 24112640, 24982842, 25074526, 25158988, 25681615, 26558335, 27067486, 27710856, 29178608, 31064749 |
ClinVar |
|
F11-AS1
|
Unknown
Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations
|
2813350, 11122101, 12879434, 14717969, 15749683, 15953011, 16079124, 16835901, 17229051, 17549289, 18758779, 18832909, 19652879, 20015217, 20523169, 21668437, 21718436, 23332144, 24982842, 27067486, 31064749 |
- |
