Search Ontology:
Human Disease

prothrombin deficiency

Term ID
DOID:2235
Synonyms
  • Congenital factor II deficiency
  • Factor II deficiency
  • Hereditary factor II deficiency disease
  • hypoprothrombinemia
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. (4)
References
Ontology
Human Disease   ( DOID:2235 )
Relationships
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Genes Involved
Zebrafish Models