Familial hemophagocytic lymphohistiocytosis 5

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the STXBP2 gene.

Also known as: FHL5, STXBP2 genetic hemophagocytic lymphohistiocytosis, familial hemophagocytic lymphohistiocytosis type 5, genetic hemophagocytic lymphohistiocytosis caused by mutation in STXBP2, hemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease, hemophagocytic lymphohistiocytosis, familial, type 5, hemophagocytic lymphohistiocytosis, familial, 5

41 clinical trials for this condition and its sub-types, 0 tagged with Familial hemophagocytic lymphohistiocytosis 5 itself.