41040004: Complete trisomy 21 syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Autosomal chromosomal disorder\Autosomal duplication\Trisomy and partial trisomy of autosome\Complete trisomy 21 syndrome
• \Chromosomal disorder\Duplication of chromosome\Autosomal duplication\Trisomy and partial trisomy of autosome\Complete trisomy 21 syndrome
• \Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 21\Complete trisomy 21 syndrome
• \Chromosomal disorder\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Complete trisomy 21 syndrome
• \Congenital disease\Congenital anomaly\Complete trisomy 21 syndrome
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 21\Complete trisomy 21 syndrome
• \Congenital disease\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Complete trisomy 21 syndrome
• \Developmental disorder\Congenital anomaly\Complete trisomy 21 syndrome

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
1229711010	T21 - Trisomy 21	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2921053011	Downs syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
68470016	Complete trisomy 21 syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
68471017	Down syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
68472012	Mongolism	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
777783010	Complete trisomy 21 syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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