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726393006: Deletion of long arm of chromosome 19 (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3463924012 Deletion of long arm of chromosome 19 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3463925013 Deletion of long arm of chromosome 19 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of long arm of chromosome 19 (disorder) localisation d'une constatation (attribut) Chromosome pair 19 (cell structure) true Inferred relationship Some 2
Deletion of long arm of chromosome 19 (disorder) est un(e) (attribut) Deletion of part of chromosome 19 (disorder) true Inferred relationship Some
Deletion of long arm of chromosome 19 (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Deletion of long arm of chromosome 19 (disorder) survenue (attribut) congénital true Inferred relationship Some 3
Deletion of long arm of chromosome 19 (disorder) morphologie associée (attribut) Deletion of long arm true Inferred relationship Some 2
Deletion of long arm of chromosome 19 (disorder) localisation d'une constatation (attribut) Long arm of chromosome (cell structure) false Inferred relationship Some 2
Deletion of long arm of chromosome 19 (disorder) morphologie associée (attribut) Partial monosomy (morphologic abnormality) true Inferred relationship Some 3
Deletion of long arm of chromosome 19 (disorder) localisation d'une constatation (attribut) Chromosome pair 19 (cell structure) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
19q13.11 microdeletion syndrome (disorder) est un(e) (attribut) True Deletion of long arm of chromosome 19 (disorder) Inferred relationship Some

This concept is not in any reference sets

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