439701000: hereditaire heparinecofactor II-deficiëntie (aandoening)

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

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

\Hereditary thrombophilia (disorder)\Hereditary heparin cofactor II deficiency (disorder)

\Heparin cofactor II deficiency\Hereditary heparin cofactor II deficiency (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Hereditary heparin cofactor II deficiency (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary heparin cofactor II deficiency (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Heparin cofactor II deficiency\Hereditary heparin cofactor II deficiency (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2788435014 Hereditary heparin cofactor II deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2794143018 Hereditary heparin cofactor II deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

7404031000146113 erfelijke deficiëntie van heparinecofactor II nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

8586231000146113 hereditaire heparinecofactor II-deficiëntie (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

8720661000146110 hereditaire heparinecofactor II-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 heparin cofactor II deficiency (disorder)	Is a	Hereditary thrombophilia (disorder)	true	Inferred relationship	Some
Hereditary heparin cofactor II deficiency (disorder)	Is a	Heparin cofactor II deficiency	true	Inferred relationship	Some
Hereditary heparin cofactor II deficiency (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary heparin cofactor II deficiency (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

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Characteristic

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Group

This concept is not in any reference sets