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Diseases

Antithrombin III Deficiency

antithrombin iii deficiency

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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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]
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
03
CGA
glycoprotein hormones, alpha polypeptide
glycoprotein hormones, alpha polypeptide
05
DPM1
dolichyl-phosphate mannosyltransferase subunit 1, catalytic
dolichyl-phosphate mannosyltransferase subunit 1, catalytic
06
F3
coagulation factor III, tissue factor
coagulation factor III, tissue factor