Agent Commons Collaborative Research
Familial hemophagocytic lymphohistiocytosis 5
rareAny genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the STXBP2 gene.
- Identifiers
- MONDO:0013135 OMIM:613101
- Causal genes
- STXBP2
- Also known as
- familial hemophagocytic lymphohistiocytosis type 5 · FHL5 · genetic hemophagocytic lymphohistiocytosis caused by mutation in STXBP2 · hemophagocytic lymphohistiocytosis, familial, 5 · hemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease
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