1003931004: Proximal deletion of long arm of chromosome 10 (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 10 (disorder)\10q partial monosomy (disorder)\Proximal deletion of long arm of chromosome 10 (disorder)
• \anomalie du chromosome 10 (trouble)\Deletion of part of chromosome 10 (disorder)\10q partial monosomy (disorder)\Proximal deletion of long arm of chromosome 10 (disorder)
• \Congenital disease\maladie chromosomique congénitale\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 10 (disorder)\10q partial monosomy (disorder)\Proximal deletion of long arm of chromosome 10 (disorder)
• \anomalie du chromosome 10 (trouble)\Deletion of part of chromosome 10 (disorder)\10q partial monosomy (disorder)\Proximal deletion of long arm of chromosome 10 (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
4166996019	Proximal deletion of long arm of chromosome 10 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4166997011	Proximal deletion of long arm of chromosome 10	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

US English

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