405769009: Klinefelter's syndrome, XXY (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - male phenotype\Klinefelter syndrome\Klinefelter's syndrome, XXY
• \Anomaly of chromosome X\Klinefelter syndrome\Klinefelter's syndrome, XXY
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - male phenotype\Klinefelter syndrome\Klinefelter's syndrome, XXY
• \Anomaly of chromosome X\Klinefelter syndrome\Klinefelter's syndrome, XXY

Status: current, Primitive. Date: 31-Jan 2004. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2149599019	Klinefelter's syndrome, XXY (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core
2157545011	Klinefelter's syndrome, XXY	en	Synonym	Active	Case sensitive	SNOMED CT core
2163147012	Klinefelter's syndrome	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
2163148019	XXY syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2163149010	Klinefelter syndrome	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
2163150010	Klinefelter's syndrome karyotype 47 XXY	en	Synonym	Active	Case sensitive	SNOMED CT core
2163151014	XXY Klinefelter's syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
2838565019	Klinefelter syndrome, XXY	en	Synonym	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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