Term Name:	thrombophilia due to HRG deficiency
Synonyms:	hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency, hereditary thrombophilia due to congenital HRG deficiency, THPH11
Definition:	A thrombophilia characterized by decreased histidine-rich glycoprotein (HRG) plasma levels and a tendency to develop thrombosis that has_material_basis_in heterozygous mutation in HRG on chromosome 3q27.3.
Ontology:	Human Disease [DOID:0111903]   ( DOID:0111903 )