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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Heterozygous prothrombin G20210A mutation (disorder) interprète (attribut) Hemostatic function (observable entity) true Inferred relationship Some 1
Heterozygous prothrombin G20210A mutation (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
Heterozygous prothrombin G20210A mutation (disorder) est un(e) (attribut) Prothrombin G20210A mutation (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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