Autosomal recessive hereditary disorder	Inherited mucociliary clearance defect
\|	\|

Cystic fibrosis (disorder)
	Cystic fibrosis
	Mucoviscidosis CF - Cystic fibrosis CF Fibrocystic disease
	cystische fibrose
	taaislijmziekte
	cystic fibrosis
	Aangeboren erfelijke ziekte met als kenmerk afscheiding van taai slijm in met name luchtwegen en alvleesklier; de medische term voor deze ziekte is cystic fibrosis of cystische fibrose.

Id	190905008
Status	Primitive

Has interpretation	Impaired
Interprets	Mucociliary clearance

Associated morphology	Defect
Finding site	Respiratory tract structure

PALGA thesaurus simple reference set for pathology

General Practice / Family Practice reference set

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	E84.9
Rule	TRUE
Advice	ALWAYS E84.9
Correlation	SNOMED CT source code to target map code correlation not specified

|

Atypical cystic fibrosis

Classical cystic fibrosis

Cystic fibrosis of pancreas1

Cystic fibrosis of the lung1

Cystic fibrosis with atypical mycobacterial infection

Cystic fibrosis with gastritis and megaloblastic anemia syndrome

Cystic fibrosis with gastritis and megaloblastic anemia syndrome

Cystic fibrosis with intestinal findings3

Cystic fibrosis with liver disease

Cystic fibrosis with meconium ileus

Cystic fibrosis with nasal polyp

Cystic fibrosis with pseudomonas infection

Cystic fibrosis without meconium ileus

Diabetes mellitus associated with cystic fibrosis

Fetal cystic fibrosis

Follicular hamartoma with alopecia and cystic fibrosis syndrome

Subclinical cystic fibrosis