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Core Information
Disease Name
Antithrombin III Deficiency
Standard Disease Name
antithrombin iii deficiency
MeSH Tree
No data
ICD-10
D68.59
Identifiers
DO ID
No data
MeSH ID
D020152
OMIM ID
613118
UMLS ID
C0272375
HPO ID
No data
Description and Extensions
Description
NCI2016_02D:A rare disorder characterized by the presence of low levels of antithrombin III which prohibits the formation of blood clots. It may be inherited, usually in an autosomal dominant pattern, or acquired. It may lead to venous thrombosis and pulmonary embolism.|MSH2017_2016_08_12:An absence or reduced level of Antithrombin III leading to an increased risk for thrombosis.|HPO2016_07_04:An abnormality of coagulation related to a decreased concentration of antithrombin-III. [HPO:probinson]
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