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403760006: XXYY syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771686011 XXYY syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1782770018 XXYY syndrome 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
XXYY syndrome (disorder) est un(e) (attribut) maladie chromosomique congénitale true Inferred relationship Some
XXYY syndrome (disorder) survenue (attribut) congénital false Inferred relationship Some
XXYY syndrome (disorder) morphologie associée (attribut) Alteration of chromosome structure false Inferred relationship Some
XXYY syndrome (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
XXYY syndrome (disorder) localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 1
XXYY syndrome (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some
XXYY syndrome (disorder) localisation d'une constatation (attribut) Chromosome structure (cell structure) false Inferred relationship Some 1
XXYY syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 1
XXYY syndrome (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
XXYY syndrome (disorder) localisation d'une constatation (attribut) Chromosome structure (cell structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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