Hemophagocytic lymphohistiocytosis due to RhoG deficiency

MONDO:0800147

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is an autosomal recessive variation in the RHOG gene.

41 clinical trials for this condition and its sub-types, 0 tagged with Hemophagocytic lymphohistiocytosis due to RhoG deficiency itself.

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