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12399004: Chromosome pair 5 (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
21339016 Chromosome pair 5 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1185979011 Chromosome pair 5 (cell structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
21339016 Chromosome pair 5 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
21339016 Chromosome pair 5 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
727380013 Chromosome pair 5 (body structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1185979011 Chromosome pair 5 (cell structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1185979011 Chromosome pair 5 (cell structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chromosome pair 5 Is a Chromosome true Inferred relationship Existential restriction modifier (core metadata concept)
Chromosome pair 5 partie de Nucleus false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Anomaly of chromosome pair 5 (disorder) Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial trisomy Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial trisomy Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 5 (disorder) Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial trisomy Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 5 (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5p partial monosomy syndrome (disorder) Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
The newly described 5q14.3 microdeletion syndrome includes severe intellectual deficit with no speech, stereotypic movements and epilepsy. Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
The newly described 5q14.3 microdeletion syndrome includes severe intellectual deficit with no speech, stereotypic movements and epilepsy. Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 3
5q35 microduplication syndrome (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion 5q35 (disorder) Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
Deletion 5q35 (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 3
Deletion of part of chromosome 5 (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of long arm of chromosome 5 (disorder) Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
Deletion of part of long arm of chromosome 5 (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 3
Partial trisomy of chromosome 5 (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Partial trisomy of long arm of chromosome 5 Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
Mosaic trisomy 5 syndrome Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
Mosaic trisomy 5 syndrome Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal trisomy 5q syndrome (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Ring chromosome 5 syndrome Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Tetrasomy 5p syndrome (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5q31.3 microdeletion syndrome Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5q31.3 microdeletion syndrome Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 3
Paternal uniparental disomy of chromosome 5 Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5p13 microduplication syndrome (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
5q22.2 deletion syndrome Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
5q22.2 deletion syndrome Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
Medial duplication of long arm of chromosome 5 (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Medial deletion of long arm of chromosome 5 (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Medial deletion of long arm of chromosome 5 (disorder) Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
Proximal duplication of long arm of chromosome 5 (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Proximal deletion of long arm of chromosome 5 Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Proximal deletion of long arm of chromosome 5 Finding site False Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
Tetrasomy 5p mosaicism (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Tetrasomy 5p mosaicism (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 2
Partial deletion of short arm of chromosome 5 Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
The newly described 5q14.3 microdeletion syndrome includes severe intellectual deficit with no speech, stereotypic movements and epilepsy. Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1
Joint contractures, developmental delay, Pierre Robin syndrome (disorder) Finding site True Chromosome pair 5 Inferred relationship Existential restriction modifier (core metadata concept) 1

This concept is not in any reference sets

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