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205655003: Trisomy 22 (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
315397013 Trisomy 22 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591053014 Trisomy 22 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
315397013 Trisomy 22 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315397013 Trisomy 22 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591053014 Trisomy 22 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591053014 Trisomy 22 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4886121000241119 trisomie 22 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4886121000241119 trisomie 22 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


8 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Trisomy 22 Is a Trisomy and partial trisomy of autosome true Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 22 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 22 Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 22 Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 22 Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 22 Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 22 Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 22 Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 22 Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 22 Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 22 Is a Anomaly of chromosome pair 22 true Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 22 Finding site Chromosome pair 22 true Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 22 Associated morphology Trisomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Partial trisomy of chromosome 22 (disorder) Is a True Trisomy 22 Inferred relationship Existential restriction modifier (core metadata concept)
Mosaic trisomy 22 syndrome Is a True Trisomy 22 Inferred relationship Existential restriction modifier (core metadata concept)
Complete trisomy 22 syndrome (disorder) Is a True Trisomy 22 Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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