Familial hemophagocytic lymphohistiocytosis 2

Definition

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

Also known as familial hemophagocytic lymphohistiocytosis type 2, FHL2, genetic hemophagocytic lymphohistiocytosis caused by mutation in PRF1, hemophagocytic lymphohistiocytosis, familial, type 2, HLH2, HPLH2, PRF1 genetic hemophagocytic lymphohistiocytosis — per MONDO

Also identified as

• DOID 0110922 per MONDO
• MESH C537250 per MONDO
• OMIM 603553 per MONDO
• UMLS C1863727 per MONDO