Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Cystic_fibrosis> ?p ?o. }
Showing items 1 to 82 of
82
with 100 items per page.
- Cystic_fibrosis abstract "Cystic fibrosis (CF), also known as mucoviscidosis, is an autosomal recessive genetic disorder that affects most critically the lungs, and also the pancreas, liver, and intestine. It is characterized by abnormal transport of chloride and sodium across an epithelium, leading to thick, viscous secretions.The name cystic fibrosis refers to the characteristic scarring (fibrosis) and cyst formation within the pancreas, first recognized in the 1930s. Difficulty breathing is the most serious symptom and results from frequent lung infections that are treated with antibiotics and other medications. Other symptoms—including sinus infections, poor growth, and infertility—affect other parts of the body.CF is caused by a frameshift mutation in the gene for the protein cystic fibrosis transmembrane conductance regulator (CFTR). This protein is required to regulate the components of sweat, digestive fluids, and mucus. CFTR regulates the movement of chloride and sodium ions across epithelial membranes, such as the alveolar epithelia located in the lungs. Most people without CF have two working copies of the CFTR gene, and both copies must be missing for CF to develop, due to the disorder's recessive nature. CF develops when neither copy works normally (as a result of mutation) and therefore has autosomal recessive inheritance.CF is most common among people of Central and Northern European ancestry, but occurs in many demographic groups around the world. The prevalence of CF is the rarest in Asia and the Middle East. Individuals with cystic fibrosis can be diagnosed before birth by genetic testing, or by a sweat test in early childhood. Ultimately, lung transplantation is often necessary as CF worsens.".
- Cystic_fibrosis diseasesdb "3347".
- Cystic_fibrosis emedicineSubject "ped".
- Cystic_fibrosis emedicineTopic "535".
- Cystic_fibrosis icd10 "E84in".
- Cystic_fibrosis icd9 "277.0".
- Cystic_fibrosis medlineplus "000107".
- Cystic_fibrosis meshId "D003550".
- Cystic_fibrosis omim "219700".
- Cystic_fibrosis thumbnail ClubbingCF.JPG?width=300.
- Cystic_fibrosis wikiPageExternalLink pmidlookup?view=long&pmid=12471090.
- Cystic_fibrosis wikiPageExternalLink pmidlookup?view=long&pmid=17082494.
- Cystic_fibrosis wikiPageExternalLink pmidlookup?view=long&pmid=12626341.
- Cystic_fibrosis wikiPageExternalLink 4448.
- Cystic_fibrosis wikiPageExternalLink cf-week.
- Cystic_fibrosis wikiPageExternalLink results.
- Cystic_fibrosis wikiPageExternalLink app.
- Cystic_fibrosis wikiPageExternalLink pmidlookup?view=long&pmid=17404297.
- Cystic_fibrosis wikiPageExternalLink 219700.
- Cystic_fibrosis wikiPageExternalLink pmidlookup?view=long&pmid=19918082.
- Cystic_fibrosis wikiPageID "50601".
- Cystic_fibrosis wikiPageRevisionID "606713866".
- Cystic_fibrosis caption "Clubbing in the fingers of a person with cystic fibrosis".
- Cystic_fibrosis diseasesdb "3347".
- Cystic_fibrosis emedicinesubj "ped".
- Cystic_fibrosis emedicinetopic "535".
- Cystic_fibrosis hasPhotoCollection Cystic_fibrosis.
- Cystic_fibrosis icd "277".
- Cystic_fibrosis icd "E84in".
- Cystic_fibrosis medlineplus "107".
- Cystic_fibrosis meshid "D003550".
- Cystic_fibrosis name "Cystic fibrosis".
- Cystic_fibrosis omim "219700".
- Cystic_fibrosis wordnet_type synset-disease-noun-1.
- Cystic_fibrosis subject Category:Autosomal_recessive_disorders.
- Cystic_fibrosis subject Category:Channelopathy.
- Cystic_fibrosis subject Category:Congenital_disorders.
- Cystic_fibrosis subject Category:Cystic_fibrosis.
- Cystic_fibrosis subject Category:Lung_disorders.
- Cystic_fibrosis subject Category:Pancreas_disorders.
- Cystic_fibrosis subject Category:Pediatrics.
- Cystic_fibrosis subject Category:Rare_diseases.
- Cystic_fibrosis subject Category:Steatorrhea-related_diseases.
- Cystic_fibrosis type Disease.
- Cystic_fibrosis type AilmentCondition.
- Cystic_fibrosis type Situation.
- Cystic_fibrosis comment "Cystic fibrosis (CF), also known as mucoviscidosis, is an autosomal recessive genetic disorder that affects most critically the lungs, and also the pancreas, liver, and intestine. It is characterized by abnormal transport of chloride and sodium across an epithelium, leading to thick, viscous secretions.The name cystic fibrosis refers to the characteristic scarring (fibrosis) and cyst formation within the pancreas, first recognized in the 1930s.".
- Cystic_fibrosis label "Cystic fibrosis".
- Cystic_fibrosis label "Fibrose cística".
- Cystic_fibrosis label "Fibrosi cistica".
- Cystic_fibrosis label "Fibrosis quística".
- Cystic_fibrosis label "Mucoviscidose".
- Cystic_fibrosis label "Mukoviszidose".
- Cystic_fibrosis label "Mukowiscydoza".
- Cystic_fibrosis label "Taaislijmziekte".
- Cystic_fibrosis label "Муковисцидоз".
- Cystic_fibrosis label "تليف كيسي".
- Cystic_fibrosis label "嚢胞性線維症".
- Cystic_fibrosis label "囊腫性纖維化".
- Cystic_fibrosis sameAs Cystická_fibróza.
- Cystic_fibrosis sameAs Mukoviszidose.
- Cystic_fibrosis sameAs Κυστική_ίνωση.
- Cystic_fibrosis sameAs Fibrosis_quística.
- Cystic_fibrosis sameAs Fibrosi_kistiko.
- Cystic_fibrosis sameAs Mucoviscidose.
- Cystic_fibrosis sameAs Fibrosis_sistik.
- Cystic_fibrosis sameAs Fibrosi_cistica.
- Cystic_fibrosis sameAs 嚢胞性線維症.
- Cystic_fibrosis sameAs 낭포성_섬유증.
- Cystic_fibrosis sameAs Taaislijmziekte.
- Cystic_fibrosis sameAs Mukowiscydoza.
- Cystic_fibrosis sameAs Fibrose_cística.
- Cystic_fibrosis sameAs Cystic_Fibrosis.
- Cystic_fibrosis sameAs m.0dcp_.
- Cystic_fibrosis sameAs Q178194.
- Cystic_fibrosis sameAs Q178194.
- Cystic_fibrosis sameAs 297.
- Cystic_fibrosis sameAs C0010674.
- Cystic_fibrosis wasDerivedFrom Cystic_fibrosis?oldid=606713866.
- Cystic_fibrosis depiction ClubbingCF.JPG.
- Cystic_fibrosis isPrimaryTopicOf Cystic_fibrosis.
- Cystic_fibrosis name "Cystic fibrosis".