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441420000: homozygote protrombine-G20210A-mutatie (aandoening)

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

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

\Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Prothrombin G20210A mutation (disorder)\Homozygous prothrombin G20210A mutation (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Prothrombin G20210A mutation (disorder)\Homozygous prothrombin G20210A mutation (disorder)
\Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Prothrombin G20210A mutation (disorder)\Homozygous 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
Homozygous prothrombin G20210A mutation (disorder)	Is a	Prothrombin G20210A mutation (disorder)	true	Inferred relationship	Some
Homozygous prothrombin G20210A mutation (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Homozygous prothrombin G20210A mutation (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
2787282019	Homozygous prothrombin G20210A mutation (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2795461010	Homozygous prothrombin G20210A mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6674641000146119	homozygote 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)
6674651000146116	homozygote 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)
7405821000146116	homozygote 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)
7700581000146119	homozygote 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)
7700591000146117	homozygote 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)
7700601000146110	homozygote 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)
7700611000146112	homozygote 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)
7700641000146113	homozygote 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)