859041000000103: Exacerbation of cystic fibrosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Functional finding\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Exacerbation of cystic fibrosis

\Respiratory finding\Disorder of respiratory system\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Exacerbation of cystic fibrosis

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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 01-Apr 2013. Module: SNOMED CT United Kingdom clinical extension module

Descriptions:

Id Description Lang Type Status Case? Module

2222551000000113 Exacerbation of cystic fibrosis (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module

2222561000000111 Exacerbation of cystic fibrosis en Synonym Active Only initial character case insensitive SNOMED CT United Kingdom clinical extension module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Exacerbation of cystic fibrosis	Is a	Cystic fibrosis	true	Inferred relationship	Existential restriction modifier
Exacerbation of cystic fibrosis	Has interpretation	Impaired	true	Inferred relationship	Existential restriction modifier	1
Exacerbation of cystic fibrosis	Interprets	Mucociliary clearance, function	true	Inferred relationship	Existential restriction modifier	1
Exacerbation of cystic fibrosis	Associated morphology	Defect	true	Inferred relationship	Existential restriction modifier	2
Exacerbation of cystic fibrosis	Finding site	Respiratory tract structure	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets