25610001: Chromosome pair 20 (cell structure)

SNOMED CT Concept\structure corporelle\Anatomical or acquired body structure (body structure)\Anatomical structure\Cell structure (cell structure)\Subcellular structure\Chromosome structure (cell structure)\Chromosome (cell structure)\Chromosome pair 20 (cell structure)

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

1187274012 Chromosome pair 20 (cell structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

42933017 Chromosome pair 20 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chromosome pair 20 (cell structure)	est un(e) (attribut)	Chromosome (cell structure)	true	Inferred relationship	Some
Chromosome pair 20 (cell structure)	partie de	Nucleus (cell structure)	false	Additional relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
20p13 microdeletion syndrome	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20p13 microdeletion syndrome	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Distal monosomy 20q	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Distal monosomy 20q	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20p12.2 deletion syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20p12.2 deletion syndrome (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Paternal 20q13.2q13.3 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20q13.33 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20p12.3 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20q11.2 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Posterior polymorphous corneal dystrophy (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Congenital hereditary endothelial dystrophy (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Congenital hereditary endothelial dystrophy type 1 (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
dystrophie endothéliale congénitale héréditaire type II	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20q partial trisomy (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20p partial trisomy syndrome	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Complete trisomy 20 syndrome (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Posterior polymorphous corneal dystrophy (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Anomaly of chromosome pair 20	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Ring chromosome 20 syndrome	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20q partial trisomy (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Congenital hereditary endothelial dystrophy (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Ring chromosome 20 syndrome	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Anomaly of chromosome pair 20	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Posterior polymorphous corneal dystrophy (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Complete trisomy 20 syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Congenital hereditary endothelial dystrophy type 1 (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
20p partial trisomy syndrome	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
dystrophie endothéliale congénitale héréditaire type II	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
20p partial trisomy syndrome	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Maternal uniparental disomy of chromosome 20 (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Paternal uniparental disomy of chromosome 20 (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20p12.3 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
20p12.3 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	3
Paternal 20q13.2q13.3 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Paternal 20q13.2q13.3 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	3
Deletion of part of chromosome 20 (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Deletion of part of long arm of chromosome 20 (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Deletion of part of long arm of chromosome 20 (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	3
Deletion of part of short arm of chromosome 20 (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Deletion of part of short arm of chromosome 20 (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	3
trisomie partielle du chromosome 20	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20q13.33 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
20q13.33 microdeletion syndrome (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	3
20q partial trisomy (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Ring chromosome 20 syndrome	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Complete trisomy 20 syndrome (disorder)	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
20q11.2 microduplication syndrome	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Distal trisomy 20q syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Mosaic trisomy 20 syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	2
Mosaic trisomy 20 syndrome (disorder)	localisation d'une constatation (attribut)	True	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1
Anomaly of chromosome pair 20	localisation d'une constatation (attribut)	False	Chromosome pair 20 (cell structure)	Inferred relationship	Some	1

Reference Sets

Description inactivation indicator reference set

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Id	Description	Lang	Type	Status	Case?	Module
1187274012	Chromosome pair 20 (cell structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
42933017	Chromosome pair 20	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core