439699000: Hereditary antithrombin III deficiency (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\...

\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary antithrombin III deficiency (disorder)
\Thrombophilia\Antithrombin III deficiency\Hereditary antithrombin III deficiency (disorder)

\Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Antithrombin III deficiency\Hereditary antithrombin III deficiency (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Hereditary antithrombin III deficiency (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary antithrombin III deficiency (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Antithrombin III deficiency\Hereditary antithrombin III deficiency (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Antithrombin III deficiency\Hereditary antithrombin III deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2788736011 Hereditary antithrombin III deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2791100010 Hereditary antithrombin III deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2425711000052113 ärftlig brist på antitrombin III sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary antithrombin III deficiency (disorder)	Is a	Hereditary thrombophilia (disorder)	true	Inferred relationship	Some
Hereditary antithrombin III deficiency (disorder)	Is a	Antithrombin III deficiency	true	Inferred relationship	Some
Hereditary antithrombin III deficiency (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary antithrombin III deficiency (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

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This concept is not in any reference sets