771340007: 15q11.2 microdeletion 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 15\Partial deletion of long arm of chromosome 15\15q11.2 microdeletion syndrome
• \Anomaly of chromosome pair 15\Deletion of part of chromosome 15\Partial deletion of long arm of chromosome 15\15q11.2 microdeletion syndrome
• \Congenital disease\Congenital malformation\15q11.2 microdeletion 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 15\Partial deletion of long arm of chromosome 15\15q11.2 microdeletion syndrome
• \Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 15\Deletion of part of chromosome 15\Partial deletion of long arm of chromosome 15\15q11.2 microdeletion syndrome
• \Developmental disorder\Congenital malformation\15q11.2 microdeletion syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3705825012	Monosomy 15q11.2	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3705826013	15q11.2 microdeletion syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3705827016	15q11.2 microdeletion syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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