OMOP Concept 441267
Cystic fibrosis
StandardConditionSNOMED190905008Disorder
Maps from
39
Descendants
15
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
39 source codes normalize to Cystic fibrosis via the OMOP "Maps to" relationship.
Showing 25 of 39 source codes. Retrieve the full set via the API.
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
(15)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 due to cystic fibrosis
- 1Exacerbation of cystic fibrosis
- 1Fetal cystic fibrosis
- 1Follicular hamartoma with alopecia and cystic fibrosis syndrome
- 1Subclinical cystic fibrosis
- 2Exocrine pancreatic manifestation co-occurrent and due to cystic fibrosis
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