JSON

cystic fibrosis

^ http://purl.obolibrary.org/obo/DOID_1485


An autosomal recessive disease that is characterized by the buildup of thick, sticky mucus that can damage many organs. [ url:http://www.nhlbi.nih.gov/health/health-topics/topics/cf/ url:http://ghr.nlm.nih.gov/condition/cystic-fibrosis url:http://en.wikipedia.org/wiki/Cystic_fibrosis ]

Synonyms: CF, mucoviscidosis

Term info

database cross reference
  • ICD9CM:277.0
  • MESH:D003550
  • ICD10CM:E84
  • ICD10CM:E84.9
  • NCI:C2975
  • SNOMEDCT_US_2018_03_01:85809002
  • GARD:6233
  • UMLS_CUI:C0010674
  • OMIM:219700
Subsets

NCIthesaurus

comment

OMIM mapping confirmed by DO. [SN].

has alternative id

DOID:1484, DOID:12447, DOID:14395, DOID:13383

has obo namespace

disease_ontology

id

DOID:1485

Term relations

Subclass of: