439699000: hereditaire antitrombine III-deficiëntie (aandoening)

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

\Procedure related finding\Evaluation finding\...

\Abnormal finding on evaluation procedure\Serum/plasma protein finding abnormal\Antithrombin III deficiency\Hereditary antithrombin III deficiency (disorder)

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

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

\Protein level - finding\Finding of protein in serum or plasma\Serum/plasma protein finding abnormal\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)

\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\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\Blood coagulation disorder\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:

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

8636971000146119 hereditaire antitrombine III-deficiëntie (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

8720381000146113 hereditaire antitrombine III-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

13546371000146112 erfelijke AT-III-deficiëntie nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands 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
Hereditary antithrombin III deficiency (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Hereditary antithrombin III deficiency (disorder)	Interprets	Plasma antithrombin III activity	true	Inferred relationship	Some	2
Hereditary antithrombin III deficiency (disorder)	Has interpretation	Abnormally low (qualifier value)	true	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

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Group

This concept is not in any reference sets