880078001: 11p15 deletion 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 11\11p partial monosomy syndrome\11p15 deletion syndrome
• \Anomaly of chromosome pair 11\Deletion of part of chromosome 11\11p partial monosomy syndrome\11p15 deletion syndrome
• \Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\11p15 deletion 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 11\11p partial monosomy syndrome\11p15 deletion syndrome
• \Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 11\Deletion of part of chromosome 11\11p partial monosomy syndrome\11p15 deletion syndrome
• \Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\11p15 deletion syndrome

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
3994437010	11p15 deletion syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3994438017	11p15 deletion syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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