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441421001: 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:

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
2425771000052118 heterozygot protrombin G20210A-mutation sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

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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