86555001: Cystic fibrosis of the lung (disorder)

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

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

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

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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cystic fibrosis of the lung	Is a	Cystic fibrosis	true	Inferred relationship	Some
Cystic fibrosis of the lung	Is a	Disorder of lower respiratory system (disorder)	false	Inferred relationship	Some
Cystic fibrosis of the lung	Finding site	Lung structure	true	Inferred relationship	Some	3
Cystic fibrosis of the lung	Is a	Disorder of lung (disorder)	true	Inferred relationship	Some
Cystic fibrosis of the lung	Associated morphology	Defect	false	Inferred relationship	Some	1
Cystic fibrosis of the lung	Finding site	Respiratory tract structure	false	Inferred relationship	Some	1
Cystic fibrosis of the lung	Has interpretation	Impaired	true	Inferred relationship	Some	2
Cystic fibrosis of the lung	Interprets	Mucociliary clearance	true	Inferred relationship	Some	2

Inbound Relationships

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Characteristic

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This concept is not in any reference sets