205686009: Karyotype 46, X iso (Xq) (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Turner syndrome\Karyotype 46, X iso (Xq)
• \Anomaly of chromosome X\Turner syndrome\Karyotype 46, X iso (Xq)
• \Congenital disease (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Turner syndrome\Karyotype 46, X iso (Xq)
• \Anomaly of chromosome X\Turner syndrome\Karyotype 46, X 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
315437010	Karyotype 46, X iso (Xq)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
591088014	Karyotype 46, X iso (Xq) (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5878311000172118	cariotype 46, X, iso Xq	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
4498741000172114	syndroom van Turner met karyotype 46,X iso (Xq)	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
4498751000172111	karyotype 46,X iso (Xq)	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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