Term Name:	familial hemophagocytic lymphohistiocytosis 2
Synonyms:	FHL2, HLH2, HPLH2
Definition:	A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of the PRF1 gene on chromosome 10q22.1.
Ontology:	Human Disease [DOID:0110922]   ( DOID:0110922 )