22053006: Klinefelter syndrome (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Fetal and/or neonatal disorder\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - male phenotype\A male with two or more X chromosomes.
• \Anomaly of chromosome X\A male with two or more X chromosomes.
• \Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - male phenotype\A male with two or more X chromosomes.
• \Anomaly of chromosome X\A male with two or more X chromosomes.

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3037904019	A male with two or more X chromosomes.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
37000018	Klinefelter syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
481209015	Klinefelter's syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
751418017	Klinefelter syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

Back to Start