86555001: Cystic fibrosis of the lung (disorder)

SNOMED CT Concept\constatation clinique\...

\Viscus structure finding (finding)\constatation à propos d'un poumon\affection du poumon (trouble)\Cystic fibrosis of the lung

\constatation à propos d'une structure du tronc\Finding of upper trunk (finding)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\affection du poumon (trouble)\Cystic fibrosis of the lung
\constatation à propos d'une structure du tronc\Finding of upper trunk (finding)\Finding of region of thorax\constatation à propos d'un poumon\affection du poumon (trouble)\Cystic fibrosis of the lung
\constatation à propos d'une structure du tronc\Finding of upper trunk (finding)\Finding of region of thorax\Disorder of thorax (disorder)\affection du poumon (trouble)\Cystic fibrosis of the lung
\constatation à propos d'une structure du tronc\affection du tronc\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\affection du poumon (trouble)\Cystic fibrosis of the lung

\constatation fonctionnelle\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung

\Respiratory finding\constatation à propos des voies respiratoires inférieures\constatation à propos d'un poumon\affection du poumon (trouble)\Cystic fibrosis of the lung
\Respiratory finding\Disorder of respiratory system (disorder)\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung
\Respiratory finding\Disorder of respiratory system (disorder)\Disorder of lower respiratory system (disorder)\affection du poumon (trouble)\Cystic fibrosis of the lung

\Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung
\Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Cystic fibrosis\Cystic fibrosis of the lung
\Disease\affection d'un système corporel\Hereditary disorder by system\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung
\Disease\affection d'un système corporel\Disorder of respiratory system (disorder)\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung
\Disease\affection d'un système corporel\Disorder of respiratory system (disorder)\Disorder of lower respiratory system (disorder)\affection du poumon (trouble)\Cystic fibrosis of the lung
\Disease\affection du tronc\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\affection du poumon (trouble)\Cystic fibrosis of the lung

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

143537016 Cystic fibrosis of the lung en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

143538014 Mucoviscidosis involving the lung en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

143539018 Pulmonary cystic fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

392871000172114 fibrose kystique du poumon fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

428271000172114 mucoviscidose avec atteinte pulmonaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

477601000241114 maladie fibrokystique du poumon (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

534361000172112 maladie fibrokystique du poumon fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

828843013 Cystic fibrosis of the lung (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cystic fibrosis of the lung	est un(e) (attribut)	affection du poumon (trouble)	true	Inferred relationship	Some
Cystic fibrosis of the lung	est un(e) (attribut)	Cystic fibrosis	true	Inferred relationship	Some
Cystic fibrosis of the lung	est un(e) (attribut)	Disorder of lower respiratory system (disorder)	false	Inferred relationship	Some
Cystic fibrosis of the lung	morphologie associée (attribut)	Defect	true	Inferred relationship	Some	1
Cystic fibrosis of the lung	localisation d'une constatation (attribut)	structure des voies respiratoires	true	Inferred relationship	Some	1
Cystic fibrosis of the lung	a pour interprétation (attribut)	altéré	true	Inferred relationship	Some	2
Cystic fibrosis of the lung	interprète (attribut)	Mucociliary clearance	true	Inferred relationship	Some	2
Cystic fibrosis of the lung	localisation d'une constatation (attribut)	structure d'un poumon	true	Inferred relationship	Some	3

Inbound Relationships

Type

Active

Source

Characteristic

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Group

Reference Sets

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