205687000: Karyotype 46, X with abnormal sex chromosome except iso (Xq) (disorder)

• SNOMED CT Concept\constatation clinique\Disease\...
• \anomalie chromosomique\maladie chromosomique congénitale\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\syndrome de Turner\Karyotype 46, X with abnormal sex chromosome except iso (Xq)
• \Anomaly of chromosome X\syndrome de Turner\Karyotype 46, X with abnormal sex chromosome except iso (Xq)
• \Congenital disease\maladie chromosomique congénitale\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\syndrome de Turner\Karyotype 46, X with abnormal sex chromosome except iso (Xq)
• \Anomaly of chromosome X\syndrome de Turner\Karyotype 46, X with abnormal sex chromosome except iso (Xq)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
315438017	Karyotype 46, X with abnormal sex chromosome except iso (Xq)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
591089018	Karyotype 46, X with abnormal sex chromosome except iso (Xq) (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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