719666002: 6q terminal deletion 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\6q terminal deletion syndrome
• \Anomaly of chromosome pair 6\Deletion of part of chromosome 6\Deletion of part of long arm of chromosome 6\6q terminal deletion 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\6q terminal deletion syndrome
• \Anomaly of chromosome pair 6\Deletion of part of chromosome 6\Deletion of part of long arm of chromosome 6\6q terminal deletion 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
3317352014	6q terminal deletion syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3317353016	6q terminal deletion syndrome	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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