OMOP Concept 441267
Cystic fibrosis
StandardConditionSNOMED190905008Disorder
Maps from
40
Descendants
17
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
40 source codes normalize to Cystic fibrosis via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Cystic fibrosis across source vocabularies.
- CF - Cystic fibrosis
- Cystic fibrosis (disorder)
- enfermedad fibroquística
- Fibrocystic disease
- fibrosis quística
- fibrosis quística (trastorno)
- FQ - fibrosis quística
- mucoviscidosis
- Mucoviscidosis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Inherited mucociliary clearance defect
- 2Autosomal hereditary disorder
- 2Hereditary disorder by system
- 2Mucociliary clearance defect
- 3Disorder of body system
- 3Disorder of respiratory system
- 3Finding of respiratory function
- 3Hereditary disease
- 4Disease
- 4Finding of respiration
- 4Functional finding
- 4Genetic disease
- 4Respiratory finding
- 5Clinical finding
Narrower concepts
(17)Included automatically when you query with descendants.
- 1Atypical cystic fibrosis
- 1Classical cystic fibrosis
- 1Cystic fibrosis due to heterozygous deltaF508 mutation
- 1Cystic fibrosis due to homozygous deltaF508 mutation
- 1Cystic fibrosis of pancreas
- 1Cystic fibrosis of the lung
- 1Cystic fibrosis with gastritis and megaloblastic anemia syndrome
- 1Cystic fibrosis with meconium ileus
- 1Cystic fibrosis without meconium ileus
- 1Diabetes mellitus associated with cystic fibrosis
- 1Exacerbation of cystic fibrosis
- 1Fetal cystic fibrosis
- 1Follicular hamartoma with alopecia and cystic fibrosis syndrome
- 1Pulmonary exacerbation cystic fibrosis
- 1Subclinical cystic fibrosis
- 2Cystic fibrosis exacerbation
- 2Exocrine pancreatic manifestation co-occurrent and due to cystic fibrosis
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