Search Ontology:
Human Disease

thrombophilia due to thrombin defect

Term ID
DOID:0111907
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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