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25610001: Chromosome pair 20 (cell structure)

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
42933017 Chromosome pair 20 en Synonym Active Entire term case insensitive SNOMED CT core module
1187274012 Chromosome pair 20 (cell structure) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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