1003901005: Proximal deletion of long arm of chromosome 18 (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 18 (disorder)\Deletion of long arm of chromosome 18\18q partial monosomy syndrome (disorder)\Proximal deletion of long arm of chromosome 18
• \anomalie du chromosome 18 (trouble)\Deletion of part of chromosome 18 (disorder)\Deletion of long arm of chromosome 18\18q partial monosomy syndrome (disorder)\Proximal deletion of long arm of chromosome 18
• \Congenital disease\maladie chromosomique congénitale\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 18 (disorder)\Deletion of long arm of chromosome 18\18q partial monosomy syndrome (disorder)\Proximal deletion of long arm of chromosome 18
• \anomalie du chromosome 18 (trouble)\Deletion of part of chromosome 18 (disorder)\Deletion of long arm of chromosome 18\18q partial monosomy syndrome (disorder)\Proximal deletion of long arm of chromosome 18

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
4166925012	Proximal deletion of long arm of chromosome 18	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4166926013	Proximal deletion of long arm of chromosome 18 (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)

US English

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