721881008: Microduplication Xp11.22p11.23 syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome X\Microduplication Xp11.22p11.23 syndrome
• \Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Microduplication Xp11.22p11.23 syndrome
• \Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome X\Microduplication Xp11.22p11.23 syndrome
• \Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Microduplication Xp11.22p11.23 syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3326431011	Microduplication Xp11.22p11.23 syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3326432016	Microduplication Xp11.22p11.23 syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3326436018	Trisomy Xp11.22-p11.23	en	Synonym	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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