762270003: Atypical cystic fibrosis (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Atypical cystic fibrosis
• \Respiratory finding\Respiratory disease\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Atypical cystic fibrosis
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Inherited mucociliary clearance defect\Cystic fibrosis\Atypical cystic fibrosis
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Cystic fibrosis\Atypical cystic fibrosis
• \Disease\Disorder of body system\Hereditary disorder by system\Inherited mucociliary clearance defect\Cystic fibrosis\Atypical cystic fibrosis
• \Disease\Disorder of body system\Respiratory disease\Mucociliary clearance defect\Inherited mucociliary clearance defect\Cystic fibrosis\Atypical cystic fibrosis

Status: current, Primitive. Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3636281015	Atypical cystic fibrosis (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3636282010	Atypical cystic fibrosis	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Respiratory finding reference set

Problem/Diagnosis reference set

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