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270889005: Deletion of long arm of chromosome 18 (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
405346013 Deletion of long arm of chromosome 18 en Synonym Active Entire term case insensitive SNOMED CT core module
405347016 18q- syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
663271013 Deletion of long arm of chromosome 18 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2108161000000114 18q deletion syndrome en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom Edition module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of long arm of chromosome 18 Is a Deletion of part of autosome false Inferred relationship Existential restriction modifier
Deletion of long arm of chromosome 18 Occurrence Congenital false Inferred relationship Existential restriction modifier
Deletion of long arm of chromosome 18 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Deletion of long arm of chromosome 18 Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Deletion of long arm of chromosome 18 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Deletion of long arm of chromosome 18 Finding site Chromosome structure false Inferred relationship Existential restriction modifier 1
Deletion of long arm of chromosome 18 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Deletion of long arm of chromosome 18 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Deletion of long arm of chromosome 18 Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Deletion of long arm of chromosome 18 Finding site Chromosome false Inferred relationship Existential restriction modifier 1
Deletion of long arm of chromosome 18 Is a Deletion of part of chromosome 18 true Inferred relationship Existential restriction modifier
Deletion of long arm of chromosome 18 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Deletion of long arm of chromosome 18 Finding site Chromosome pair 18 true Inferred relationship Existential restriction modifier 1
Deletion of long arm of chromosome 18 Finding site Chromosome pair 18 true Inferred relationship Existential restriction modifier 2
Deletion of long arm of chromosome 18 Associated morphology Deletion of long arm true Inferred relationship Existential restriction modifier 2
Deletion of long arm of chromosome 18 Occurrence Congenital true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group
18q partial monosomy syndrome Is a True Deletion of long arm of chromosome 18 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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