Term Name: familial hemophagocytic lymphohistiocytosis 5
Synonyms: FHL5, HLH5, HPLH5
Definition: A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the STXBP2 gene on chromosome 19p13.2.
Ontology: Human Disease [DOID:0110925]   ( DOID:0110925 )

Relationships
is a type of: hemophagocytic lymphohistiocytosis monogenic disease