National Cancer Institute Thesaurus

Last uploaded: February 21, 2019
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Preferred Name

Antithrombin III Deficiency
ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C98815
code

C98815
Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99147
Contributing_Source

NICHD
DEFINITION

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.
Has_NICHD_Parent

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2902
label

Antithrombin III Deficiency
NICHD_Hierarchy_Term

Antithrombin III Deficiency
Preferred_Name

Antithrombin III Deficiency
prefixIRI

C98815
prefLabel

Antithrombin III Deficiency
Semantic_Type

Disease or Syndrome
UMLS_CUI

C0272375
subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2902

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C53543
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http://purl.bioontology.org/ontology/OMIM/MTHU001757 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/OMIM/613118 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU005311 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/MESH/D020152 Medical Subject Headings LOOM
http://purl.obolibrary.org/obo/DOID_3755 Human Disease Ontology 123 LOOM