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22053006: Klinefelter syndrome (disorder)

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
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
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
37001019 XXY syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
481208011 Klinefelter's syndrome karyotype 47 XXY 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
481210013 XXY 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 Only initial character case insensitive (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
3037904019 A male with two or more X chromosomes. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
372561000274119 Klinefelter-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
818831000241115 syndrome de Klinefelter fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
818831000241115 syndrome de Klinefelter fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
372561000274119 Klinefelter-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
A male with two or more X chromosomes. Is a Anomaly of chromosome X false Inferred relationship Existential restriction modifier (core metadata concept)
A male with two or more X chromosomes. Is a Sex chromosome abnormality - male phenotype false Inferred relationship Existential restriction modifier (core metadata concept)
A male with two or more X chromosomes. Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
A male with two or more X chromosomes. Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier (core metadata concept)
A male with two or more X chromosomes. Finding site Sex chromosome X (cell structure) false Inferred relationship Existential restriction modifier (core metadata concept)
A male with two or more X chromosomes. Is a Sex chromosome abnormality - male phenotype true Inferred relationship Existential restriction modifier (core metadata concept)
A male with two or more X chromosomes. Is a Anomaly of chromosome X true Inferred relationship Existential restriction modifier (core metadata concept)
A male with two or more X chromosomes. Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
A male with two or more X chromosomes. Associated morphology Alteration of chromosome structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
A male with two or more X chromosomes. Finding site Sex chromosome X (cell structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Klinefelter's syndrome - male with more than two X chromosomes Is a False A male with two or more X chromosomes. Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XXYY (disorder) Is a False A male with two or more X chromosomes. Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XY/XXY mosaic Is a False A male with two or more X chromosomes. Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome NOS Is a False A male with two or more X chromosomes. Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XXY (disorder) Is a True A male with two or more X chromosomes. Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome XXXY Is a True A male with two or more X chromosomes. Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome XXXXY Is a True A male with two or more X chromosomes. Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XXYY (disorder) Is a True A male with two or more X chromosomes. Inferred relationship Existential restriction modifier (core metadata concept)
Klinefelter's syndrome, XY/XXY mosaic Is a True A male with two or more X chromosomes. Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set

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