cystic fibrosis

Preferred Label : cystic fibrosis;

MeSH definition : An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.;

MeSH synonym : fibrosis, cystic; mucoviscidosis;

CISMeF synonym : CF;

MeSH hyponym : pulmonary cystic fibrosis; pancreatic cystic fibrosis; Cystic Fibrosis, Pulmonary; Cystic Fibrosis, Pancreatic; Fibrocystic Disease of Pancreas; Pancreas Fibrocystic Disease; Pancreas Fibrocystic Diseases; Cystic Fibrosis of Pancreas;

MeSH annotation : a specific disease entity: do not use for fibrocystic states of various organs;

Wikipedia link : https://en.wikipedia.org/wiki/Cystic fibrosis;

Details

Origin ID

D003550;

UMLS CUI

C0010674;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Currated CISMeF NLP mapping
- CYSTIC FIBROSIS PANCREATIC [WHO-ART Included Term]
- Cystic Fibrosis [NCIt concept]
- Cystic fibrosis [PASCAL descriptor]
- Cystic fibrosis [ICD-10 category]
- Cystic fibrosis [LOINC component]
- Cystic fibrosis [ICD-11 Category]
- Cystic fibrosis [ICD-10 category (who)]
- Cystic fibrosis [MedDRA Preferred Term]
- Cystic fibrosis [HPMULTI term]
- Cystic fibrosis [OMIM Phenotype]
- Cystic fibrosis [ACR pathology]
- Cystic fibrosis [ACR pathology]
- Cystic fibrosis [ORDO Disease]
- Cystic fibrosis (disorder) [SNOMED CT concept]
- Cystic fibrosis NOS [MedDRA LLT]
- Cystic fibrosis of pancreas (disorder) [SNOMED CT concept]
- Cystic fibrosis pancreas [MedDRA LLT]
- Cystic fibrosis pancreatic [MedDRA Preferred Term]
- Disease fibrocystic pancreas [MedDRA LLT]
- MUCOVISCIDOSIS [WHO-ART Included Term]
- Mucoviscidosis [MedDRA LLT]
- cystic fibrosis [DO Concept]
- cystic fibrosis [Disease (Nov.)]
- cystic fibrosis [MedlinePlus Topic]
- cystic fibrosis [SNOMED Notion]
- cystic fibrosis [TUV Concept]
- cystic fibrosis [TUV Term]
- cystic fibrosis [Artificial nutrition thesaurus concept]
- cystic fibrosis [Radlex concept]
- cystic fibrosis of the pancreas [Disease (Nov.)]
DO Cross reference
- cystic fibrosis [DO Concept]
False automatic mappings
- Cisplatin/Fluorouracil Regimen [NCIt concept]
- Congo [NCIt concept]
Indexing information
- CLCA4 protein, human [MeSH Supplementary Concept]
- DNASE1 protein, human [MeSH Supplementary Concept]
- MucA protein, pseudomonas [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Genetic pancreatic disease [ORDO Disease]
- Male infertility due to obstructive azoospermia [ORDO Disease]
- Non-pore-loop channelopathy due to epithelial Cl- channel CFTR anomaly [ORDO Disease]
- Rare genetic respiratory disease [ORDO Disease]
- Rare male infertility [ORDO Disease]
- Rare pancreatic disease [ORDO Disease]
- Rare pulmonary disease [ORDO Disease]
MedlinePlus topic(s)
- cystic fibrosis [MedlinePlus Topic]
ORDO relation(s)
- Cystic fibrosis [ORDO Disease]
Record concept(s)
- cystic fibrosis [MeSH concept]
- pancreatic cystic fibrosis [MeSH concept]
- pulmonary cystic fibrosis [MeSH concept]
Related MeSH Supplementary Concept(s)
- cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and subnormal mentality [MeSH Supplementary Concept]
- follicular hamartoma alopecia cystic fibrosis [MeSH Supplementary Concept]
- lubani al saleh teebi syndrome [MeSH Supplementary Concept]
See also
- cystic fibrosis transmembrane conductance regulator [MeSH Descriptor]
- mice, inbred cftr [MeSH Descriptor]
- sweating [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CYSTIC FIBROSIS PANCREATIC [WHO-ART Included Term]
- Cystic Fibrosis [NCIt concept]
- Cystic fibrosis [MedDRA Preferred Term]
- Cystic fibrosis [OMIM Phenotype]
- Cystic fibrosis [ICD-9 code]
- Cystic fibrosis [ORDO Disease]
- Cystic fibrosis [ICD-10 category]
- Cystic fibrosis [ACR pathology]
- Cystic fibrosis [ACR pathology]
- Cystic fibrosis [ICD-10 category (who)]
- Cystic fibrosis [LOINC component]
- Cystic fibrosis [PASCAL descriptor]
- Cystic fibrosis (disorder) [SNOMED CT concept]
- Cystic fibrosis NOS [MedDRA LLT]
- Cystic fibrosis, unspecified [ICD-10 Sub-category]
- MUCOVISCIDOSIS [WHO-ART Included Term]
- Mucoviscidosis [MedDRA LLT]
- cystic fibrosis [Radlex concept]
- cystic fibrosis [TUV Concept]
- cystic fibrosis [TUV Term]
- cystic fibrosis [SNOMED Notion]
- cystic fibrosis [DO Concept]
- cystic fibrosis [Disease (Nov.)]
- cystic fibrosis [MedlinePlus Topic]
Validated automatic mappings to BTNT
- pulmonary cystic fibrosis [Disease (Nov.)]

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