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441421001: heterozygote protrombine-G20210A-mutatie (aandoening)

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

\Functional finding\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Prothrombin G20210A mutation (disorder)\Heterozygous prothrombin G20210A mutation (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Prothrombin G20210A mutation (disorder)\Heterozygous prothrombin G20210A mutation (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Prothrombin G20210A mutation (disorder)\Heterozygous prothrombin G20210A mutation (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Prothrombin G20210A mutation (disorder)\Heterozygous prothrombin G20210A mutation (disorder)

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Heterozygous prothrombin G20210A mutation (disorder)	Is a	Prothrombin G20210A mutation (disorder)	true	Inferred relationship	Some
Heterozygous prothrombin G20210A mutation (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Heterozygous prothrombin G20210A mutation (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

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
2787283012	Heterozygous prothrombin G20210A mutation (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2790996019	Heterozygous prothrombin G20210A mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6674661000146118	heterozygote protrombine-G20210A-mutatie	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6674671000146112	heterozygote protrombine-G20210A-mutatie (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
7405071000146111	heterozygote mutatie van protrombine G20210A	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
7700361000146116	heterozygote G20210A-mutatie van stollingsfactor II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
7700371000146110	heterozygote G20210A-mutatie van factor II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
7700381000146112	heterozygote G20210A-mutatie van bloedstollingsfactor II	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
7700391000146114	heterozygote G20210A-protrombinemutatie	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
7700401000146112	heterozygote G20210A-mutatie van protrombine	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)