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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

42 clinical trials for this condition and its sub-types, 1 tagged with Familial hemophagocytic lymphohistiocytosis 3 itself.

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