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726399005: Deletion of part of chromosome 22 (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3448867011 Deletion of part of chromosome 22 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448868018 Deletion of part of chromosome 22 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448867011 Deletion of part of chromosome 22 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448868018 Deletion of part of chromosome 22 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5836091000241119 délétion d'une partie du chromosome 22 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5836101000241111 délétion partielle du chromosome 22 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5836091000241119 délétion d'une partie du chromosome 22 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5836101000241111 délétion partielle du chromosome 22 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of chromosome 22 (disorder) Is a Anomaly of chromosome pair 22 true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 22 (disorder) Is a Deletion of part of autosome true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 22 (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 22 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 22 (disorder) Finding site Chromosome pair 22 true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
22q partial monosomy Is a True Deletion of part of chromosome 22 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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