123648007: Chromosomal alterations of group C and X (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Fetal and/or neonatal disorder\Congenital disease\Congenital chromosomal disease\Group chromosomal alteration\Chromosomal alterations of group C and X
• \Chromosomal disorder (disorder)\Congenital chromosomal disease\Group chromosomal alteration\Chromosomal alterations of group C and X

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
192137018	Chromosomal alterations of group C and X	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
726618011	Chromosomal alterations of group C and X (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5741371000241111	altérations chromosomiques des groupes C et X	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5741381000241113	altérations des chromosomes de 6 à 12 et du chromosome X	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

US English

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