Search Ontology:
Human Disease

thrombophilia due to HRG deficiency

Term ID
DOID:0111903
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. (2)
References
Ontology
Human Disease   ( DOID:0111903 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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