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205651007: Trisomy 10 (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
315393012 Trisomy 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591049012 Trisomy 10 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
315393012 Trisomy 10 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315393012 Trisomy 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
591049012 Trisomy 10 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
591049012 Trisomy 10 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4886061000241110 trisomie 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4886061000241110 trisomie 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Trisomy 10 (disorder) Is a Trisomy and partial trisomy of autosome true Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 10 (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 10 (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 10 (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 10 (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 10 (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 10 (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 10 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 10 (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 10 (disorder) Finding site Chromosome structure (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 10 (disorder) Is a Anomaly of chromosome pair 10 (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Trisomy 10 (disorder) Finding site Chromosome pair 10 true Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy 10 (disorder) Associated morphology Trisomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Trisomy 10p (disorder) Is a True Trisomy 10 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Partial trisomy of chromosome 10 (disorder) Is a True Trisomy 10 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Mosaic trisomy 10 syndrome (disorder) Is a True Trisomy 10 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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