205615000: Trisomy 21- meiotic nondisjunction (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
315346017	Trisomy 21- meiotic nondisjunction	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
591009016	Trisomy 21- meiotic nondisjunction (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5830061000172117	trisomie 21 - non-disjonction méiotique	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
5048131000172112	trisomie 21 door meiotische non-disjunctie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
5048141000172117	syndroom van Down door non-disjunctie tijdens meiose	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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