Version: 8.0.0
Date: Tue Jan 28 2025
prothrombin deficiency
DOID:2235
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

prothrombin deficiency

Definition
A thrombophilia that is characterized by bleeding symptoms due to low levels of circulating prothrombin, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding coagulation factor II, also known as prothrombin, on chromosome 11p11.
Synonyms
  • Congenital factor II deficiency
  • Factor II deficiency
Cross References
Parent Terms
Child Terms
None
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