Term Name: familial hemophagocytic lymphohistiocytosis 3
Synonyms: FHL3, HLH3, HPLH3
Definition: A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the UNC13D gene on chromosome 17q25.1.
Ontology: Human Disease [DOID:0110923]   ( DOID:0110923 )

Relationships
is a type of: autosomal recessive disease hemophagocytic lymphohistiocytosis