Familial hemophagocytic lymphohistiocytosis 4

MONDO:0011336

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the STX11 gene.

Also known as: FHL4, HLH4, HPLH4, STX11 genetic hemophagocytic lymphohistiocytosis, familial hemophagocytic lymphohistiocytosis 4, familial hemophagocytic lymphohistiocytosis type 4, genetic hemophagocytic lymphohistiocytosis caused by mutation in STX11, hemophagocytic lymphohistiocytosis, familial, type 4

41 clinical trials for this condition and its sub-types, 0 tagged with Familial hemophagocytic lymphohistiocytosis 4 itself.

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↑ Hereditary hemophagocytic lymphohistiocytosis (16)

Including sub-types (41) Tagged with Familial hemophagocytic lymphohistiocytosis 4 (0)

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