Familial hemophagocytic lymphohistiocytosis 3

Definition

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the UNC13D gene.

Also known as familial hemophagocytic lymphohistiocytosis type 3, FHL3, genetic hemophagocytic lymphohistiocytosis caused by mutation in UNC13D, hemophagocytic lymphohistiocytosis, familial, type 3, HLH3, HPLH3, UNC13D genetic hemophagocytic lymphohistiocytosis — per MONDO

Also identified as

• DOID 0110923 per MONDO
• MESH C537251 per MONDO
• OMIM 608898 per MONDO
• UMLS C1837174 per MONDO