763061004: 20q11.2 microduplication syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Autosomal chromosomal disorder\Autosomal duplication\Trisomy and partial trisomy of autosome\Partial trisomy of chromosome 20\20q partial trisomy\20q11.2 microduplication syndrome
• \Chromosomal disorder\Duplication of chromosome\Autosomal duplication\Trisomy and partial trisomy of autosome\Partial trisomy of chromosome 20\20q partial trisomy\20q11.2 microduplication syndrome
• \Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 20\Partial trisomy of chromosome 20\20q partial trisomy\20q11.2 microduplication syndrome
• \Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Partial trisomy of chromosome 20\20q partial trisomy\20q11.2 microduplication syndrome
• \Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\20q11.2 microduplication syndrome
• \Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 20\Partial trisomy of chromosome 20\20q partial trisomy\20q11.2 microduplication syndrome
• \Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Partial trisomy of chromosome 20\20q partial trisomy\20q11.2 microduplication syndrome
• \Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\20q11.2 microduplication syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3637731017	20q11.2 microduplication syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3637732012	20q11.2 microduplication 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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