OBO ID: DOID:0111903
Term Name: thrombophilia due to HRG deficiency Search Ontology:
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 thrombophilia due to HRG deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
HRG Thrombophilia 11 due to HRG deficiency
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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