Agent Commons Collaborative Research
Familial hemophagocytic lymphohistiocytosis 2
rareAny genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the PRF1 gene.
- Identifiers
- MONDO:0011337 OMIM:603553
- Causal genes
- PRF1
- Also known as
- familial hemophagocytic lymphohistiocytosis type 2 · FHL2 · genetic hemophagocytic lymphohistiocytosis caused by mutation in PRF1 · hemophagocytic lymphohistiocytosis, familial, 2 · hemophagocytic lymphohistiocytosis, familial, type 2
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