1003911003: Proximal deletion of short arm of chromosome 9 (disorder)

• SNOMED CT Concept\constatation clinique\Disease\...
• \anomalie chromosomique\maladie chromosomique congénitale\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 9 (disorder)\Proximal deletion of short arm of chromosome 9
• \anomalie du chromosome 9 (trouble)\Deletion of part of chromosome 9 (disorder)\Proximal deletion of short arm of chromosome 9
• \Congenital disease\maladie chromosomique congénitale\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 9 (disorder)\Proximal deletion of short arm of chromosome 9
• \anomalie du chromosome 9 (trouble)\Deletion of part of chromosome 9 (disorder)\Proximal deletion of short arm of chromosome 9

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
4166950010	Proximal deletion of short arm of chromosome 9	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4166951014	Proximal deletion of short arm of chromosome 9 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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