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loading...| Preferred Name |
prothrombin deficiency |
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| Synonyms |
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| 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. |
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| ID |
http://purl.obolibrary.org/obo/DOID_2235 |
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| 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. |
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| label |
prothrombin deficiency |
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| prefixIRI |
DOID:2235 |
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| prefLabel |
prothrombin deficiency |
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| subClassOf |
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