Term Name: | thrombophilia due to HRG deficiency |
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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 ) |