Link to this page
FNS-Harmony
Last uploaded:
November 2, 2023
Jump to:
| Preferred Name | prothrombin deficiency | |
| Synonyms |
|
|
| Definitions |
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. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_2235 |
|
| 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.
|
|
| imported from | ||
| label |
prothrombin deficiency
|
|
| prefixIRI |
DOID:2235
|
|
| prefLabel |
prothrombin deficiency
|
|
| subClassOf |
Add comment
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |
Create mapping