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726392001: Deletion of part of chromosome 19 (disorder)


Status: current, Defined. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3448853019 Deletion of part of chromosome 19 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3448854013 Deletion of part of chromosome 19 en Synonym Active Case insensitive SNOMED CT core


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of chromosome 19 Is a Anomaly of chromosome pair 19 true Inferred relationship Some
Deletion of part of chromosome 19 Is a Deletion of part of autosome true Inferred relationship Some
Deletion of part of chromosome 19 Associated morphology Partial monosomy true Inferred relationship Some 1
Deletion of part of chromosome 19 Occurrence Congenital true Inferred relationship Some 1
Deletion of part of chromosome 19 Finding site Chromosome pair 19 true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
19p13.12 microdeletion syndrome Is a False Deletion of part of chromosome 19 Inferred relationship Some
19q13.11 microdeletion syndrome Is a False Deletion of part of chromosome 19 Inferred relationship Some
Deletion of long arm of chromosome 19 Is a True Deletion of part of chromosome 19 Inferred relationship Some
Deletion of short arm of chromosome 19 Is a True Deletion of part of chromosome 19 Inferred relationship Some
19p13.13 microdeletion syndrome Is a False Deletion of part of chromosome 19 Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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