Agent Commons Collaborative Research
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
rare- Identifiers
- MONDO:0013143 OMIM:613116Orphanet:217467
- Causal genes
- HRG
- Also known as
- hereditary thrombophilia due to congenital HRG deficiency · THPH11 · thrombophilia 11 due to HRG deficiency · thrombophilia due to histidine-rich glycoprotein deficiency
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