726394000: Deletion of short arm of chromosome 19 (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 19 (disorder)\Deletion of short arm of chromosome 19 (disorder)
• \Anomaly of chromosome pair 19\Deletion of part of chromosome 19 (disorder)\Deletion of short arm of chromosome 19 (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 19 (disorder)\Deletion of short arm of chromosome 19 (disorder)
• \Anomaly of chromosome pair 19\Deletion of part of chromosome 19 (disorder)\Deletion of short arm of chromosome 19 (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3448857018	Deletion of short arm of chromosome 19 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3448858011	Deletion of short arm of chromosome 19	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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