86555001: Cystic fibrosis of the lung (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Viscus structure finding (finding)\Lung finding\Disease of lung (disorder)\Cystic fibrosis of the lung

\Finding of trunk structure\Finding of upper trunk (finding)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disease of lung (disorder)\Cystic fibrosis of the lung
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Lung finding\Disease of lung (disorder)\Cystic fibrosis of the lung
\Finding of trunk structure\Finding of upper trunk (finding)\Finding of region of thorax\Disorder of thorax (disorder)\Disease of lung (disorder)\Cystic fibrosis of the lung
\Finding of trunk structure\Disorder of trunk (disorder)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disease of lung (disorder)\Cystic fibrosis of the lung

\Functional finding\Finding of respiratory function (finding)\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung

\Respiratory finding\Finding of respiration\Finding of respiratory function (finding)\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung
\Respiratory finding\Lower respiratory tract finding\Lung finding\Disease of lung (disorder)\Cystic fibrosis of the lung
\Respiratory finding\Disorder of respiratory system\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung
\Respiratory finding\Disorder of respiratory system\Disease of lower respiratory system\Disease of lung (disorder)\Cystic fibrosis of the lung

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Cystic fibrosis\Cystic fibrosis of the lung
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung
\Disease\Disorder of body system\Disorder of respiratory system\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Cystic fibrosis of the lung
\Disease\Disorder of body system\Disorder of respiratory system\Disease of lower respiratory system\Disease of lung (disorder)\Cystic fibrosis of the lung
\Disease\Disorder of trunk (disorder)\Disorder of thoracic segment of trunk\Disorder of thorax (disorder)\Disease of lung (disorder)\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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cystic fibrosis of the lung	Is a	Cystic fibrosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Cystic fibrosis of the lung	Is a	Disease of lower respiratory system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Cystic fibrosis of the lung	Finding site	Lung structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Cystic fibrosis of the lung	Is a	Disease of lung (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Cystic fibrosis of the lung	Associated morphology	Defect	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Cystic fibrosis of the lung	Finding site	Respiratory tract structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Cystic fibrosis of the lung	Has interpretation	Impaired (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Cystic fibrosis of the lung	Interprets	Mucociliary clearance	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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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
828843013	Cystic fibrosis of the lung (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
143537016	Cystic fibrosis of the lung	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
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	Only initial character 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	Only initial character 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
828843013	Cystic fibrosis of the lung (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
828843013	Cystic fibrosis of the lung (disorder)	en	Fully specified name	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 Switzerland NRC maintained Module
428271000172114	mucoviscidose avec atteinte pulmonaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
534361000172112	maladie fibrokystique du poumon	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
392871000172114	fibrose kystique du poumon	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
428271000172114	mucoviscidose avec atteinte pulmonaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
534361000172112	maladie fibrokystique du poumon	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module