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1003905001: Proximal duplication of chromosome 21 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4166935018 Proximal duplication of chromosome 21 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4166936017 Proximal duplication of chromosome 21 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4823101000052110 proximal duplikation av kromosom 21 sv Synonym (core metadata concept) Active Entire term 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
Proximal duplication of chromosome 21 (disorder) Is a Partial trisomy of chromosome 21 true Inferred relationship Some
Proximal duplication of chromosome 21 (disorder) Occurrence Congenital true Inferred relationship Some 1
Proximal duplication of chromosome 21 (disorder) Finding site Chromosome pair 21 true Inferred relationship Some 1
Proximal duplication of chromosome 21 (disorder) Associated morphology Partial trisomy 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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