890127007: 7p21.1 deletion syndrome (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)\7p21.1 deletion syndrome
• \anomalie du chromosome 7 (trouble)\Deletion of part of chromosome 7 (disorder)\7p partial monosomy (disorder)\7p21.1 deletion syndrome
• \Congenital disease\Congenital malformation\7p21.1 deletion syndrome
• \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)\7p21.1 deletion syndrome
• \Congenital disease\maladie chromosomique congénitale\Anomaly of chromosome pair\anomalie du chromosome 7 (trouble)\Deletion of part of chromosome 7 (disorder)\7p partial monosomy (disorder)\7p21.1 deletion syndrome
• \trouble du développement\Congenital malformation\7p21.1 deletion syndrome

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
4009219010	7p21.1 deletion syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4009220016	7p21.1 deletion syndrome (disorder)	en	Fully specified name	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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