1003913000: Proximal deletion of short arm of chromosome 7 (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 7 (disorder)\7p partial monosomy (disorder)\Proximal deletion of short arm of chromosome 7 (disorder)
• \anomalie du chromosome 7 (trouble)\Deletion of part of chromosome 7 (disorder)\7p partial monosomy (disorder)\Proximal deletion of short arm of chromosome 7 (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 7 (disorder)\7p partial monosomy (disorder)\Proximal deletion of short arm of chromosome 7 (disorder)
• \anomalie du chromosome 7 (trouble)\Deletion of part of chromosome 7 (disorder)\7p partial monosomy (disorder)\Proximal deletion of short arm of chromosome 7 (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
4166954018	Proximal deletion of short arm of chromosome 7 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4166955017	Proximal deletion of short arm of chromosome 7	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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