890128002: 9p24.3 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 9\Distal monosomy 9p syndrome\9p24.3 deletion syndrome
• \Anomaly of chromosome pair 9\Deletion of part of chromosome 9\Distal monosomy 9p syndrome\9p24.3 deletion syndrome
• \Congenital disease\Congenital malformation\9p24.3 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 9\Distal monosomy 9p syndrome\9p24.3 deletion syndrome
• \Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 9\Deletion of part of chromosome 9\Distal monosomy 9p syndrome\9p24.3 deletion syndrome
• \Developmental disorder\Congenital malformation\9p24.3 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
4009221017	9p24.3 deletion syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
4009222012	9p24.3 deletion syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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