699254009: Microdeletion of chromosome 15q13.3 (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\Microdeletion of chromosome 15q13.3
• \Anomaly of chromosome pair 15\Deletion of part of chromosome 15\Partial deletion of long arm of chromosome 15\Microdeletion of chromosome 15q13.3
• \Congenital disease\Congenital anomaly\Microdeletion of chromosome 15q13.3
• \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\Microdeletion of chromosome 15q13.3
• \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\Microdeletion of chromosome 15q13.3
• \Developmental disorder\Congenital anomaly\Microdeletion of chromosome 15q13.3

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2983307014	15q13.3 deletion syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
2983429014	15q13.3 microdeletion	en	Synonym	Active	Case insensitive	SNOMED CT core
2983673017	Microdeletion of chromosome 15q13.3 (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3015079019	Microdeletion of chromosome 15q13.3	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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