Hereditary hemophagocytic lymphohistiocytosis

MONDO:0015541

An instance of hemophagocytic lymphohistiocytosis that is caused by an inherited genomic modification in an individual.

Also known as: familial hemophagocytic lymphohistiocytosis, genetic hemophagocytic lymphohistiocytosis, genetic hemophagocytic syndrome, primary hemophagocytic lymphohistiocytosis

61 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by