OBO ID: DOID:0111907
Term Name: thrombophilia due to thrombin defect Search Ontology:
Synonyms:
  • prothrombin-related thrombophilia
  • THPH1
  • thrombophilia due to factor 2 defect
Definition: A thrombophilia characterized by recurrent thrombophilia that has_material_basis_in heterozygous mutation in F2 on chromosome 11p11.2. (2)
References:
Ontology: Human Disease   ( DOID:0111907 )
Relationships
is a type of:
OTHER thrombophilia due to thrombin defect PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
F13A1 {Venous thrombosis, protection against} 188050
F2 Thrombophilia 1 due to thrombin defect 188050
HABP2 {Venous thromboembolism, susceptibility to} 188050
MTHFR {Thromboembolism, susceptibility to} 188050
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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