439699000: Hereditary antithrombin III deficiency (disorder)

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

\Procedure related finding\Evaluation finding\...

\Abnormal finding on evaluation procedure\Antithrombin III deficiency\Hereditary antithrombin III deficiency (disorder)

\Measurement finding\Finding of substance level (finding)\...

\Finding of blood substance level (finding)\Finding of protein in serum or plasma\Antithrombin III deficiency\Hereditary antithrombin III deficiency (disorder)

\Finding of protein level (finding)\Finding of protein in serum or plasma\Antithrombin III deficiency\Hereditary antithrombin III deficiency (disorder)

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

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

\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\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\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary 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\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Deficiency of naturally occurring coagulation factor inhibitor\Antithrombin III deficiency\Hereditary antithrombin III deficiency (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

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	Existential restriction modifier (core metadata concept)
Hereditary antithrombin III deficiency (disorder)	Is a	Antithrombin III deficiency	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary antithrombin III deficiency (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary antithrombin III deficiency (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary antithrombin III deficiency (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary antithrombin III deficiency (disorder)	Interprets	Plasma antithrombin III activity	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary antithrombin III deficiency (disorder)	Has interpretation	Abnormally low (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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
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
3390811001000112	Hereditäre Thrombophilie durch kongenitalen Antithrombin-Mangel	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5935151000241110	déficit en antithrombine III, héréditaire	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5935161000241113	déficit héréditaire en antithrombine III	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5935171000241117	déficit héréditaire en AT III	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5935181000241115	thrombophilie héréditaire due au déficit congénital en antithrombine 3	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5935151000241110	déficit en antithrombine III, héréditaire	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5935161000241113	déficit héréditaire en antithrombine III	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5935171000241117	déficit héréditaire en AT III	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5935181000241115	thrombophilie héréditaire due au déficit congénital en antithrombine 3	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3390811001000112	Hereditäre Thrombophilie durch kongenitalen Antithrombin-Mangel	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module