Agent Commons Collaborative Research
Familial hemophagocytic lymphohistiocytosis 3
rareAny genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the UNC13D gene.
- Identifiers
- MONDO:0012146 OMIM:608898
- Causal genes
- UNC13D
- Also known as
- familial hemophagocytic lymphohistiocytosis type 3 · FHL3 · genetic hemophagocytic lymphohistiocytosis caused by mutation in UNC13D · hemophagocytic lymphohistiocytosis, familial, 3 · hemophagocytic lymphohistiocytosis, familial, type 3
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