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DOID:0111903 - thrombophilia due to HRG deficiency
Disease Ontology 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: THPH11, hereditary thrombophilia due to congenital HRG deficiency, hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency,
Xenbase Genes : hrg
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee