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726394000: Deletion of short arm of chromosome 19 (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
3448857018 Deletion of short arm of chromosome 19 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3448858011 Deletion of short arm of chromosome 19 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 short arm of chromosome 19 Is a Deletion of part of chromosome 19 true Inferred relationship Existential restriction modifier
Deletion of short arm of chromosome 19 Associated morphology Deletion of short arm true Inferred relationship Existential restriction modifier 2
Deletion of short arm of chromosome 19 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Deletion of short arm of chromosome 19 Finding site Short arm of chromosome false Inferred relationship Existential restriction modifier 2
Deletion of short arm of chromosome 19 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 3
Deletion of short arm of chromosome 19 Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Deletion of short arm of chromosome 19 Finding site Chromosome pair 19 true Inferred relationship Existential restriction modifier 3
Deletion of short arm of chromosome 19 Finding site Chromosome pair 19 true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
19p13.13 microdeletion syndrome Is a True Deletion of short arm of chromosome 19 Inferred relationship Existential restriction modifier
Distal monosomy 19p13.3 Is a True Deletion of short arm of chromosome 19 Inferred relationship Existential restriction modifier
19p13.12 microdeletion syndrome Is a True Deletion of short arm of chromosome 19 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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