Familial hemophagocytic lymphohistiocytosis 2

MONDO:0011337

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the PRF1 gene.

Also known as: FHL2, HLH2, HPLH2, PRF1 genetic hemophagocytic lymphohistiocytosis, familial hemophagocytic lymphohistiocytosis type 2, genetic hemophagocytic lymphohistiocytosis caused by mutation in PRF1, hemophagocytic lymphohistiocytosis, familial, type 2, Hlh2

41 clinical trials for this condition and its sub-types, 0 tagged with Familial hemophagocytic lymphohistiocytosis 2 itself.

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↑ Hereditary hemophagocytic lymphohistiocytosis (16)

Including sub-types (41) Tagged with Familial hemophagocytic lymphohistiocytosis 2 (0)

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