OBO ID: DOID:2235
Term Name: prothrombin deficiency Search Ontology:
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
is a type of:
OTHER prothrombin deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
F2 Dysprothrombinemia 613679
Hypoprothrombinemia 613679
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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