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 disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 21\Complete trisomy 21 syndrome\Trisomy 21- meiotic nondisjunction
\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction\Trisomy 21- meiotic nondisjunction
\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Complete trisomy 21 syndrome\Trisomy 21- meiotic nondisjunction

\Congenital disease\Congenital malformation\Complete trisomy 21 syndrome\Trisomy 21- meiotic nondisjunction
\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 21\Complete trisomy 21 syndrome\Trisomy 21- meiotic nondisjunction
\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction\Trisomy 21- meiotic nondisjunction
\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\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. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

315346017 Trisomy 21- meiotic nondisjunction en Synonym Active Entire term case insensitive SNOMED CT core module

591009016 Trisomy 21- meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Trisomy 21- meiotic nondisjunction	Is a	Complete trisomy 21 syndrome	true	Inferred relationship	Existential restriction modifier
Trisomy 21- meiotic nondisjunction	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	2
Trisomy 21- meiotic nondisjunction	Associated morphology	Trisomy	true	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Finding site	Sex chromosome	false	Inferred relationship	Existential restriction modifier
Trisomy 21- meiotic nondisjunction	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	2
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	2
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	2
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	2
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	2
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	false	Inferred relationship	Existential restriction modifier	2
Trisomy 21- meiotic nondisjunction	Associated morphology	Trisomy	false	Inferred relationship	Existential restriction modifier	2
Trisomy 21- meiotic nondisjunction	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier
Trisomy 21- meiotic nondisjunction	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Associated morphology	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Finding site	Chromosome pair 21	true	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Trisomy 21- meiotic nondisjunction	Is a	Whole chromosome trisomy meiotic nondisjunction	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
315346017	Trisomy 21- meiotic nondisjunction	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
591009016	Trisomy 21- meiotic nondisjunction (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module