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726397007: Deletion of part of short arm of chromosome 20 (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3467373013 Deletion of part of short arm of chromosome 20 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3467374019 Deletion of part of short arm of chromosome 20 en Synonym Active Entire term case insensitive SNOMED CT core module

3 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of short arm of chromosome 20 Is a Deletion of part of chromosome 20 true Inferred relationship Existential restriction modifier
Deletion of part of short arm of chromosome 20 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Deletion of part of short arm of chromosome 20 Finding site Chromosome pair 20 true Inferred relationship Existential restriction modifier 2
Deletion of part of short arm of chromosome 20 Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Deletion of part of short arm of chromosome 20 Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier 3
Deletion of part of short arm of chromosome 20 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
Deletion of part of short arm of chromosome 20 Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 3
Deletion of part of short arm of chromosome 20 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Deletion of part of short arm of chromosome 20 Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 1
Deletion of part of short arm of chromosome 20 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
20p12.3 microdeletion syndrome Is a True Deletion of part of short arm of chromosome 20 Inferred relationship Existential restriction modifier
20p13 microdeletion syndrome Is a True Deletion of part of short arm of chromosome 20 Inferred relationship Existential restriction modifier
20p12.2 deletion syndrome Is a True Deletion of part of short arm of chromosome 20 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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