699308002: Microdeletion of chromosome 15q24 (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 15\Partial deletion of long arm of chromosome 15\15q24 microdeletion
• \Anomaly of chromosome pair 15\Deletion of part of chromosome 15\Partial deletion of long arm of chromosome 15\15q24 microdeletion
• \Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\15q24 microdeletion
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 15\Partial deletion of long arm of chromosome 15\15q24 microdeletion
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 15\Deletion of part of chromosome 15\Partial deletion of long arm of chromosome 15\15q24 microdeletion
• \Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\15q24 microdeletion

Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2983610010	15q24 microdeletion	en	Synonym	Active	Case insensitive	SNOMED CT core
2983637012	15q24 microdeletion syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
2983648017	Interstitial deletion of chromosome 15q24	en	Synonym	Active	Case insensitive	SNOMED CT core
2983696017	Microdeletion of chromosome 15q24 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
2983720014	15q24 deletion	en	Synonym	Active	Case insensitive	SNOMED CT core
3023268018	Microdeletion of chromosome 15q24	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

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