Search Ontology:
Human Disease
prothrombin deficiency
- Term ID
- DOID:2235
- Synonyms
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- 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
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- MESH:C562724
- MIM:613679
- NCI:C26799
- ORDO:325
- SNOMEDCT_US_2023_03_01:33297000
- UMLS_CUI:C0272317
- Ontology
- Human Disease ( DOID:2235 )
- is a type of
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Genes Involved
Zebrafish Models