205623003: Trisomy 18 - 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 18 - meiotic nondisjunction
\Chromosomal disorder\Autosomal chromosomal disorder\Autosomal duplication\Trisomy and partial trisomy of autosome\Complete trisomy 18 syndrome\Trisomy 18 - meiotic nondisjunction
\Chromosomal disorder\Duplication of chromosome\Autosomal duplication\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction\Trisomy 18 - meiotic nondisjunction
\Chromosomal disorder\Duplication of chromosome\Autosomal duplication\Trisomy and partial trisomy of autosome\Complete trisomy 18 syndrome\Trisomy 18 - meiotic nondisjunction
\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 18\Complete trisomy 18 syndrome\Trisomy 18 - 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 18 - meiotic nondisjunction
\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Complete trisomy 18 syndrome\Trisomy 18 - meiotic nondisjunction

\Congenital disease\Congenital malformation\Complete trisomy 18 syndrome\Trisomy 18 - meiotic nondisjunction
\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 18\Complete trisomy 18 syndrome\Trisomy 18 - 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 18 - meiotic nondisjunction
\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Complete trisomy 18 syndrome\Trisomy 18 - meiotic nondisjunction

\Developmental disorder\Congenital malformation\Complete trisomy 18 syndrome\Trisomy 18 - 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

315354015 Trisomy 18 - meiotic nondisjunction en Synonym Active Entire term case insensitive SNOMED CT core module

591018019 Trisomy 18 - 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 18 - meiotic nondisjunction	Is a	Complete trisomy 18 syndrome	true	Inferred relationship	Existential restriction modifier
Trisomy 18 - meiotic nondisjunction	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - meiotic nondisjunction	Associated morphology	Trisomy	true	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Finding site	Sex chromosome	false	Inferred relationship	Existential restriction modifier
Trisomy 18 - meiotic nondisjunction	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - meiotic nondisjunction	Associated morphology	Trisomy	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - meiotic nondisjunction	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier
Trisomy 18 - meiotic nondisjunction	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Associated morphology	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Finding site	Chromosome pair 18	true	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - meiotic nondisjunction	Is a	Whole chromosome trisomy meiotic nondisjunction	true	Inferred relationship	Existential restriction modifier
Trisomy 18 - meiotic nondisjunction	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1

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
315354015	Trisomy 18 - meiotic nondisjunction	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
591018019	Trisomy 18 - meiotic nondisjunction (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module