Preferred Name |
cystic fibrosis |
|
Synonyms |
CF mucoviscidosis pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis cystic fibrosis cystic fibrosis lung disease, modifier of |
|
Definitions |
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. |
|
ID |
http://purl.obolibrary.org/obo/MONDO_0009061 |
|
closeMatch | ||
database_cross_reference |
NCIT:C2975 NORD:1026 UMLS:C0010674 MESH:D003550 OMIM:219700 GARD:6233 icd11.foundation:514403112 ICD9:277.0 SCTID:190905008 ICD10CM:E84 DOID:1485 Orphanet:586 MedDRA:10011762 |
|
definition |
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. |
|
exactMatch |
http://purl.obolibrary.org/obo/DOID_1485 http://identifiers.org/snomedct/190905008 http://purl.obolibrary.org/obo/Orphanet_586 http://purl.bioontology.org/ontology/ICD10CM/E84 http://identifiers.org/mesh/D003550 |
|
has_exact_synonym |
CF mucoviscidosis pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis cystic fibrosis cystic fibrosis lung disease, modifier of |
|
IAO_0000233 | ||
id |
MONDO:0009061 |
|
in_subset |
http://purl.obolibrary.org/obo/mondo#ordo_disease http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#nord_rare http://purl.obolibrary.org/obo/mondo#orphanet_rare |
|
label |
cystic fibrosis |
|
notation |
MONDO:0009061 |
|
prefLabel |
cystic fibrosis |
|
see also |
https://rarediseases.info.nih.gov/diseases/6233/cystic-fibrosis |
|
excluded_subClassOf |
http://purl.obolibrary.org/obo/MONDO_0015509 http://purl.obolibrary.org/obo/MONDO_0002356 |
|
subClassOf |