762269004: Classical cystic fibrosis (disorder)

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

\Functional finding\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Classical cystic fibrosis (disorder)

\Respiratory finding\Disorder of respiratory system (disorder)\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Classical cystic fibrosis (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Inherited mucociliary clearance defect\Cystic fibrosis\Classical cystic fibrosis (disorder)
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Cystic fibrosis\Classical cystic fibrosis (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Inherited mucociliary clearance defect\Cystic fibrosis\Classical cystic fibrosis (disorder)
\Disease\Disorder of body system\Disorder of respiratory system (disorder)\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Classical cystic fibrosis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3636279017 Classical cystic fibrosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3636280019 Classical cystic fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5498821000241113 mucoviscidose classique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Classical cystic fibrosis (disorder)	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Some
Classical cystic fibrosis (disorder)	Is a	Cystic fibrosis	true	Inferred relationship	Some
Classical cystic fibrosis (disorder)	Is a	Hereditary disorder by system	false	Inferred relationship	Some
Classical cystic fibrosis (disorder)	Has interpretation	Impaired	true	Inferred relationship	Some	2
Classical cystic fibrosis (disorder)	Interprets	Mucociliary clearance	true	Inferred relationship	Some	2
Classical cystic fibrosis (disorder)	Associated morphology	Defect	false	Inferred relationship	Some	3
Classical cystic fibrosis (disorder)	Finding site	Respiratory tract structure	false	Inferred relationship	Some	3
Classical cystic fibrosis (disorder)	Finding site	Respiratory tract structure	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Liver cirrhosis due to classical cystic fibrosis	Due to	True	Classical cystic fibrosis (disorder)	Inferred relationship	Some	4

This concept is not in any reference sets