205615000: Trisomy 21- meiotic nondisjunction (disorder)

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

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
315346017	Trisomy 21- meiotic nondisjunction	en	Synonym	Active	Case insensitive	SNOMED CT core
591009016	Trisomy 21- meiotic nondisjunction (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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