Terminology Service for NFDI4Health
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Antithrombin III Deficiency

Go to external page http://purl.obolibrary.org/obo/NCIT_C98815

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. [ ]

Term info

Label

Antithrombin III Deficiency

Synonyms
  • Antithrombin III Deficiency
Subsets

NCIT_C90259, NCIT_C99147, NCIT_C132009

ALT 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://purl.obolibrary.org/obo/NCIT_C2902

NICHD Hierarchy Term

Antithrombin III Deficiency

Preferred Name

Antithrombin III Deficiency

Semantic Type

Disease or Syndrome

UMLS CUI

C0272375

code

C98815