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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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Klinefelter's syndrome, XXY (disorder) est un(e) (attribut) Klinefelter's syndrome (disorder) false Inferred relationship Some
Klinefelter's syndrome, XXY (disorder) morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some
Klinefelter's syndrome, XXY (disorder) survenue (attribut) congénital false Inferred relationship Some
Klinefelter's syndrome, XXY (disorder) localisation d'une constatation (attribut) Sex chromosome X (cell structure) false Inferred relationship Some 1
Klinefelter's syndrome, XXY (disorder) est un(e) (attribut) Klinefelter's syndrome false Inferred relationship Some
Klinefelter's syndrome, XXY (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Klinefelter's syndrome, XXY (disorder) localisation d'une constatation (attribut) Sex chromosome X (cell structure) false Inferred relationship Some 1
Klinefelter's syndrome, XXY (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
Klinefelter's syndrome, XXY (disorder) survenue (attribut) congénital false Inferred relationship Some 1
Klinefelter's syndrome, XXY (disorder) morphologie associée (attribut) Cellular AND/OR subcellular abnormality false Inferred relationship Some 1
Klinefelter's syndrome, XXY (disorder) localisation d'une constatation (attribut) Sex chromosome X (cell structure) false Inferred relationship Some 1
Klinefelter's syndrome, XXY (disorder) est un(e) (attribut) Klinefelter syndrome true Inferred relationship Some
Klinefelter's syndrome, XXY (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Klinefelter's syndrome, XXY (disorder) morphologie associée (attribut) Alteration of chromosome structure true Inferred relationship Some 2
Klinefelter's syndrome, XXY (disorder) localisation d'une constatation (attribut) Sex chromosome X (cell structure) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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