719663005: 6q25 microdeletion syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 6\Deletion of part of long arm of chromosome 6\6q25 microdeletion syndrome
• \Anomaly of chromosome pair 6\Deletion of part of chromosome 6\Deletion of part of long arm of chromosome 6\6q25 microdeletion syndrome
• \Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 6\Deletion of part of long arm of chromosome 6\6q25 microdeletion syndrome
• \Anomaly of chromosome pair 6\Deletion of part of chromosome 6\Deletion of part of long arm of chromosome 6\6q25 microdeletion syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3317293016	6q25 microdeletion syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3317294010	6q25 microdeletion syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3317295011	Monosomy 6q25	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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