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1162440009: Deletion of part of short arm of chromosome 12 (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4589390015 Deletion of part of short arm of chromosome 12 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4589391016 Deletion of part of short arm of chromosome 12 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of short arm of chromosome 12 (disorder) est un(e) (attribut) Deletion of part of chromosome 12 (disorder) true Inferred relationship Some
Deletion of part of short arm of chromosome 12 (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Deletion of part of short arm of chromosome 12 (disorder) localisation d'une constatation (attribut) Chromosome pair 12 (cell structure) true Inferred relationship Some 1
Deletion of part of short arm of chromosome 12 (disorder) morphologie associée (attribut) Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
Deletion of part of short arm of chromosome 12 (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Deletion of part of short arm of chromosome 12 (disorder) localisation d'une constatation (attribut) Short arm of chromosome (cell structure) true Inferred relationship Some 2
Deletion of part of short arm of chromosome 12 (disorder) morphologie associée (attribut) Partial monosomy (morphologic abnormality) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Distal monosomy 12p est un(e) (attribut) True Deletion of part of short arm of chromosome 12 (disorder) Inferred relationship Some
12p12.1 microdeletion syndrome est un(e) (attribut) True Deletion of part of short arm of chromosome 12 (disorder) Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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