Familial hemophagocytic lymphohistiocytosis type 1

MONDO:0009974

Familial Hemophagocytic lymphohistiocytosis (FHL) is a rare primary immunodeficiency characterized by a macrophage activation syndrome with an onset usually occurring within a few months or less common several years after birth.

Also known as: familial hemophagocytic lymphohistiocytosis, FHL1, HLH1, HPLH1, familial HLH, familial hemophagocytic lymphohistiocytosis type 1, Erythrophagocytic lymphohistiocytosis, familial, Hlh1

41 clinical trials for this condition and its sub-types, 0 tagged with Familial hemophagocytic lymphohistiocytosis type 1 itself.

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↑ Hereditary neurological disease (5791) ↑ Hereditary hemophagocytic lymphohistiocytosis (16)

Including sub-types (41) Tagged with Familial hemophagocytic lymphohistiocytosis type 1 (0)

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