710008008: Monosomy X (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Turner syndrome\Monosomy X
• \Anomaly of chromosome X\Turner syndrome\Monosomy X
• \Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Turner syndrome\Monosomy X
• \Anomaly of chromosome X\Turner syndrome\Monosomy X

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2015. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3042484018	45XO - Turner's syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3042543019	45, X syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3042601019	XO syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3042635016	Monosomy X	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3042643014	Karyotype 45, X	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3042697014	Monosomy X (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3042710016	XO - Turner's syndrome	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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