205619006: Trisomy 13, meiotic nondisjunction (disorder)

SNOMED CT Concept\constatation clinique\Disease\...

\anomalie chromosomique\Autosomal chromosomal disorder (disorder)\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction (disorder)\Trisomy 13, meiotic nondisjunction
\anomalie chromosomique\Autosomal chromosomal disorder (disorder)\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction
\anomalie chromosomique\Duplication of chromosome\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction (disorder)\Trisomy 13, meiotic nondisjunction
\anomalie chromosomique\Duplication of chromosome\Autosomal duplication (disorder)\Trisomy and partial trisomy of autosome\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction
\anomalie chromosomique\maladie chromosomique congénitale\Anomaly of chromosome pair\Anomaly of chromosome pair 13\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction
\anomalie chromosomique\maladie chromosomique congénitale\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction (disorder)\Trisomy 13, meiotic nondisjunction
\anomalie chromosomique\maladie chromosomique congénitale\Trisomy and partial trisomy of autosome\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction

\Congenital disease\Congenital malformation\Trisomy 13, meiotic nondisjunction
\Congenital disease\maladie chromosomique congénitale\Anomaly of chromosome pair\Anomaly of chromosome pair 13\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction
\Congenital disease\maladie chromosomique congénitale\Trisomy and partial trisomy of autosome\Whole chromosome trisomy meiotic nondisjunction (disorder)\Trisomy 13, meiotic nondisjunction
\Congenital disease\maladie chromosomique congénitale\Trisomy and partial trisomy of autosome\Complete trisomy 13 syndrome\Trisomy 13, meiotic nondisjunction

\trouble du développement\Congenital malformation\Trisomy 13, 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

315350012 Trisomy 13, meiotic nondisjunction en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

591013011 Trisomy 13, meiotic nondisjunction (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Trisomy 13, meiotic nondisjunction	est un(e) (attribut)	Whole chromosome trisomy meiotic nondisjunction (disorder)	true	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	est un(e) (attribut)	Congenital malformation	true	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	morphologie associée (attribut)	Trisomy	true	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	est un(e) (attribut)	Complete trisomy 13 syndrome	true	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	morphologie associée (attribut)	Congenital anomaly	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	morphologie associée (attribut)	Congenital anomaly	false	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	morphologie associée (attribut)	Trisomy	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	survenue (attribut)	congénital	false	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	morphologie associée (attribut)	Trisomy	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Sex chromosome (cell structure)	false	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	morphologie associée (attribut)	Alteration of chromosome structure	false	Inferred relationship	Some
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	false	Inferred relationship	Some	2
Trisomy 13, meiotic nondisjunction	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	localisation d'une constatation (attribut)	Chromosome pair 13 (cell structure)	true	Inferred relationship	Some	1
Trisomy 13, meiotic nondisjunction	morphologie associée (attribut)	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Description inactivation indicator reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
315350012	Trisomy 13, meiotic nondisjunction	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
591013011	Trisomy 13, meiotic nondisjunction (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core