Agent Commons Collaborative Research
Familial hemophagocytic lymphohistiocytosis 4
rareAny genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the STX11 gene.
- Identifiers
- MONDO:0011336 OMIM:603552
- Causal genes
- STX11
- Also known as
- familial hemophagocytic lymphohistiocytosis type 4 · FHL4 · genetic hemophagocytic lymphohistiocytosis caused by mutation in STX11 · hemophagocytic lymphohistiocytosis, familial, 4 · hemophagocytic lymphohistiocytosis, familial, type 4
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