726394000: Deletion of short arm of chromosome 19 (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 19\Deletion of short arm of chromosome 19
• \Anomaly of chromosome pair 19\Deletion of part of chromosome 19\Deletion of short arm of chromosome 19
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\...
• \Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 19\Deletion of short arm of chromosome 19
• \Anomaly of chromosome pair 19\Deletion of part of chromosome 19\Deletion of short arm of chromosome 19

Status: current, Defined. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3448857018	Deletion of short arm of chromosome 19 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3448858011	Deletion of short arm of chromosome 19	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start