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405769009: Klinefelter's syndrome, XXY (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case sensitive (core metadata concept) SNOMED CT core
2157545011 Klinefelter's syndrome, XXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2163148019 XXY syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2163150010 Klinefelter's syndrome karyotype 47 XXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2163151014 XXY Klinefelter's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2838565019 Klinefelter syndrome, XXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2149599019 Klinefelter's syndrome, XXY (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2149599019 Klinefelter's syndrome, XXY (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2157545011 Klinefelter's syndrome, XXY en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2157545011 Klinefelter's syndrome, XXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2163147012 Klinefelter's syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2163148019 XXY syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2163149010 Klinefelter syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2163150010 Klinefelter's syndrome karyotype 47 XXY en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2163150010 Klinefelter's syndrome karyotype 47 XXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2163151014 XXY Klinefelter's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2838565019 Klinefelter syndrome, XXY en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2838565019 Klinefelter syndrome, XXY en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
6967581000241113 syndrome de Klinefelter, XXY fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6967581000241113 syndrome de Klinefelter, XXY fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Klinefelter's syndrome, XXY (disorder) Is a Klinefelter's syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XXY (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XXY (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XXY (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome, XXY (disorder) Is a Klinefelter's syndrome - male with more than two X chromosomes false Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XXY (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome, XXY (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome, XXY (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XXY (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome, XXY (disorder) Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome, XXY (disorder) Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Klinefelter's syndrome, XXY (disorder) Is a A male with two or more X chromosomes. true Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XXY (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Klinefelter's syndrome, XXY (disorder) Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Klinefelter's syndrome, XXY (disorder) Finding site Sex chromosome X (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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