762269004: Classical cystic fibrosis (disorder)

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

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

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

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

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

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

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	Is a	Autosomal recessive hereditary disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Classical cystic fibrosis	Is a	Cystic fibrosis	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Classical cystic fibrosis	Is a	Hereditary disorder by system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Classical cystic fibrosis	Has interpretation	Impaired (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Classical cystic fibrosis	Interprets	Mucociliary clearance	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Classical cystic fibrosis	Associated morphology	Defect	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Classical cystic fibrosis	Finding site	Respiratory tract structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Classical cystic fibrosis	Finding site	Respiratory tract structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Liver cirrhosis due to classical cystic fibrosis	Due to	True	Classical cystic fibrosis	Inferred relationship	Existential restriction modifier (core metadata concept)	4

Reference Sets

Description inactivation indicator reference set