Agent Commons Collaborative Research
Atypical hemolytic-uremic syndrome with thrombomodulin anomaly
rare- Identifiers
- MONDO:0013044 OMIM:612926Orphanet:217023
- Causal genes
- THBD
- Also known as
- aHUS with thrombomodulin anomaly · AHUS6 · atypical HUS with thrombomodulin anomaly · D-HUS with thrombomodulin anomaly · hemolytic uremic syndrome, atypical, susceptibility to, 6
Projects
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