1003910002: Proximal deletion of short arm of chromosome 8 (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 8\8p partial monosomy syndrome\Proximal deletion of short arm of chromosome 8
• \Anomaly of chromosome pair 8\Deletion of part of chromosome 8\8p partial monosomy syndrome\Proximal deletion of short arm of chromosome 8
• \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 8\8p partial monosomy syndrome\Proximal deletion of short arm of chromosome 8
• \Anomaly of chromosome pair 8\Deletion of part of chromosome 8\8p partial monosomy syndrome\Proximal deletion of short arm of chromosome 8

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4166947012	Proximal deletion of short arm of chromosome 8 (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
4166948019	Proximal deletion of short arm of chromosome 8	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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