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1003911003: Proximal deletion of short arm of chromosome 9 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4166950010 Proximal deletion of short arm of chromosome 9 en Synonym Active Entire term case insensitive SNOMED CT core module
4166951014 Proximal deletion of short arm of chromosome 9 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Proximal deletion of short arm of chromosome 9 Is a Deletion of part of chromosome 9 true Inferred relationship Existential restriction modifier
Proximal deletion of short arm of chromosome 9 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Proximal deletion of short arm of chromosome 9 Finding site Chromosome pair 9 true Inferred relationship Existential restriction modifier 1
Proximal deletion of short arm of chromosome 9 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Proximal deletion of short arm of chromosome 9 Associated morphology Deletion of short arm true Inferred relationship Existential restriction modifier 2
Proximal deletion of short arm of chromosome 9 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Proximal deletion of short arm of chromosome 9 Finding site Chromosome pair 9 true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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