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25610001: Chromosome pair 20 (cell structure)

Status: current, Primitive. 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 Case insensitive SNOMED CT core
42933017 Chromosome pair 20 en Synonym Active Case insensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chromosome pair 20 Is a Chromosome true Inferred relationship Some
Chromosome pair 20 Part of Nucleus false Additional relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
20p13 microdeletion syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
20p13 microdeletion syndrome Finding site False Chromosome pair 20 Inferred relationship Some 2
Distal monosomy 20q Finding site False Chromosome pair 20 Inferred relationship Some 2
Distal monosomy 20q Finding site False Chromosome pair 20 Inferred relationship Some 1
20p12.2 deletion syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
20p12.2 deletion syndrome Finding site False Chromosome pair 20 Inferred relationship Some 2
Paternal 20q13.2q13.3 microdeletion syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
20q13.33 microdeletion syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
20p12.3 microdeletion syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
Corneal dystrophy and perceptive deafness syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
20q11.2 microdeletion syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
Polymorphous corneal dystrophy Finding site False Chromosome pair 20 Inferred relationship Some 2
Congenital hereditary endothelial dystrophy Finding site False Chromosome pair 20 Inferred relationship Some 1
Congenital hereditary endothelial dystrophy type 1 Finding site False Chromosome pair 20 Inferred relationship Some 1
Congenital hereditary endothelial dystrophy type 2 Finding site False Chromosome pair 20 Inferred relationship Some 1
20q partial trisomy Finding site False Chromosome pair 20 Inferred relationship Some 1
20p partial trisomy syndrome Finding site False Chromosome pair 20 Inferred relationship Some 1
Complete trisomy 20 syndrome Finding site False Chromosome pair 20 Inferred relationship Some 1
Polymorphous corneal dystrophy Finding site False Chromosome pair 20 Inferred relationship Some 2
Anomaly of chromosome pair 20 Finding site False Chromosome pair 20 Inferred relationship Some 1
Ring chromosome 20 syndrome Finding site False Chromosome pair 20 Inferred relationship Some 1
20q partial trisomy Finding site True Chromosome pair 20 Inferred relationship Some 1
Congenital hereditary endothelial dystrophy Finding site True Chromosome pair 20 Inferred relationship Some 2
Ring chromosome 20 syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
Anomaly of chromosome pair 20 Finding site True Chromosome pair 20 Inferred relationship Some 1
Polymorphous corneal dystrophy Finding site False Chromosome pair 20 Inferred relationship Some 2
Complete trisomy 20 syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
Congenital hereditary endothelial dystrophy type 1 Finding site True Chromosome pair 20 Inferred relationship Some 2
20p partial trisomy syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
Congenital hereditary endothelial dystrophy type 2 Finding site True Chromosome pair 20 Inferred relationship Some 2
20p partial trisomy syndrome Finding site False Chromosome pair 20 Inferred relationship Some 1
Maternal uniparental disomy of chromosome 20 Finding site True Chromosome pair 20 Inferred relationship Some 1
Paternal uniparental disomy of chromosome 20 Finding site True Chromosome pair 20 Inferred relationship Some 1
20p12.3 microdeletion syndrome Finding site False Chromosome pair 20 Inferred relationship Some 2
20p12.3 microdeletion syndrome Finding site False Chromosome pair 20 Inferred relationship Some 3
Paternal 20q13.2q13.3 microdeletion syndrome Finding site False Chromosome pair 20 Inferred relationship Some 2
Paternal 20q13.2q13.3 microdeletion syndrome Finding site False Chromosome pair 20 Inferred relationship Some 3
Deletion of part of chromosome 20 Finding site True Chromosome pair 20 Inferred relationship Some 1
Deletion of part of long arm of chromosome 20 Finding site True Chromosome pair 20 Inferred relationship Some 2
Deletion of part of long arm of chromosome 20 Finding site False Chromosome pair 20 Inferred relationship Some 3
Deletion of part of short arm of chromosome 20 Finding site True Chromosome pair 20 Inferred relationship Some 2
Deletion of part of short arm of chromosome 20 Finding site False Chromosome pair 20 Inferred relationship Some 3
Partial trisomy of chromosome 20 Finding site True Chromosome pair 20 Inferred relationship Some 1
20q13.33 microdeletion syndrome Finding site False Chromosome pair 20 Inferred relationship Some 2
20q13.33 microdeletion syndrome Finding site False Chromosome pair 20 Inferred relationship Some 3
20q partial trisomy Finding site False Chromosome pair 20 Inferred relationship Some 1
Ring chromosome 20 syndrome Finding site False Chromosome pair 20 Inferred relationship Some 1
Complete trisomy 20 syndrome Finding site False Chromosome pair 20 Inferred relationship Some 1
20q11.2 microduplication syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
Distal trisomy 20q syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
Mosaic trisomy 20 syndrome Finding site True Chromosome pair 20 Inferred relationship Some 2
Mosaic trisomy 20 syndrome Finding site True Chromosome pair 20 Inferred relationship Some 1
Anomaly of chromosome pair 20 Finding site False Chromosome pair 20 Inferred relationship Some 1

Reference Sets

Body structure foundation reference set

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