Familial hemophagocytic lymphohistiocytosis 3

MONDO:0012146

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the UNC13D gene.

Also known as: FHL3, HLH3, HPLH3, UNC13D genetic hemophagocytic lymphohistiocytosis, familial hemophagocytic lymphohistiocytosis type 3, genetic hemophagocytic lymphohistiocytosis caused by mutation in UNC13D, hemophagocytic lymphohistiocytosis, familial, type 3, Hlh3

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