Disease

thrombophilia due to HRG deficiency

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.
Synonyms
  • hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
  • hereditary thrombophilia due to congenital HRG deficiency
Cross References
Parent Terms
Child Terms
None
Sources of Associations

Associated Genes

Associated Alleles

Associated Models