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Cystic fibrosis

^ http://www.orpha.net/ORDO/Orphanet_586


Cystic fibrosis (CF) is a genetic disorder characterized by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity.

Synonyms: Mucoviscidosis, CF

Term info

database cross reference
  • ICD-10:E84.9 (BTNT (broader term maps to a narrower term))
  • OMIM:219700 (E (exact mapping (the terms and the concepts are equivalent)))
  • MedDRA:10011762 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:E84.0 (BTNT (broader term maps to a narrower term))
  • ICD-10:E84.1 (BTNT (broader term maps to a narrower term))
  • ICD-10:E84.8 (BTNT (broader term maps to a narrower term))
  • ICD-10:E84.8 (Specific code (The term has its own code in the ICD10))
  • ICD-10:E84.1 (Specific code (The term has its own code in the ICD10))
  • ICD-10:E84.0 (Specific code (The term has its own code in the ICD10))
  • MeSH:D003550 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:E84.9 (Specific code (The term has its own code in the ICD10))
  • UMLS:C0010674 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

ICD-10:E84.8, OMIM:219700, ICD-10:E84.9, MedDRA:10011762, ICD-10:E84.0, ICD-10:E84.1, UMLS:C0010674, MeSH:D003550

notation

ORPHA:586

Term relations

Subclass of: