About: Antithrombin III Deficiency

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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

Attributes	Values
rdf:type	Class
rdfs:label	Antithrombin III Deficiency
rdfs:subClassOf	Blood Coagulation Disorders Rare Non-Neoplastic Disorder
Has_NICHD_Parent	Blood Coagulation Disorders
Concept_In_Subset	NICHD Terminology Neonatal Research Network Terminology
Semantic_Type	Disease or Syndrome
Preferred_Name	Antithrombin III Deficiency
UMLS_CUI	C0272375
Contributing_Source	NICHD
FULL_SYN	Antithrombin III DeficiencyPTNCI Antithrombin III DeficiencyPTNICHD
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.NCI
code	C98815

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