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1003915007: Proximal deletion of short arm of chromosome 3 (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
4166958015 Proximal deletion of short arm of chromosome 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4166959011 Proximal deletion of short arm of chromosome 3 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
7695411000241113 délétion proximale de 3p fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7695421000241118 délétion proximale du bras court du chromosome 3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Proximal deletion of short arm of chromosome 3 Is a 3p partial monosomy syndrome (disorder) true Inferred relationship Some
Proximal deletion of short arm of chromosome 3 Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
Proximal deletion of short arm of chromosome 3 Occurrence Congenital true Inferred relationship Some 1
Proximal deletion of short arm of chromosome 3 Finding site Chromosome pair 3 true Inferred relationship Some 1
Proximal deletion of short arm of chromosome 3 Associated morphology Deletion of short arm true Inferred relationship Some 3
Proximal deletion of short arm of chromosome 3 Finding site Chromosome pair 3 true Inferred relationship Some 3
Proximal deletion of short arm of chromosome 3 Occurrence Congenital true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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