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1003901005: Proximal deletion of long arm of chromosome 18 (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
4166925012 Proximal deletion of long arm of chromosome 18 en Synonym Active Entire term case insensitive SNOMED CT core module
4166926013 Proximal deletion of long arm of chromosome 18 (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 long arm of chromosome 18 Is a 18q partial monosomy syndrome true Inferred relationship Existential restriction modifier
Proximal deletion of long arm of chromosome 18 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Proximal deletion of long arm of chromosome 18 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Proximal deletion of long arm of chromosome 18 Finding site Chromosome pair 18 true Inferred relationship Existential restriction modifier 1
Proximal deletion of long arm of chromosome 18 Finding site Chromosome pair 18 true Inferred relationship Existential restriction modifier 3
Proximal deletion of long arm of chromosome 18 Associated morphology Deletion of long arm true Inferred relationship Existential restriction modifier 3
Proximal deletion of long arm of chromosome 18 Occurrence Congenital true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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