Preferred Name | cystic fibrosis | |
Synonyms |
mucoviscidosis pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis cystic fibrosis lung disease, modifier of cystic fibrosis CF |
|
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 |
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closeMatch | ||
exactMatch |
http://purl.obolibrary.org/obo/DOID_1485 http://identifiers.org/snomedct/190905008 http://purl.bioontology.org/ontology/ICD10CM/E84 http://www.orpha.net/ORDO/Orphanet_586 http://identifiers.org/mesh/D003550 |
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has characteristic | ||
hasDbXref |
ICD10CM:E84 Orphanet:586 OMIM:219700 UMLS:C0010674 SCTID:190905008 MESH:D003550 MedDRA:10011762 DOID:1485 GARD:6233 ICD9:277.0 NCIT:C2975 NORD:1026 |
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hasExactSynonym |
mucoviscidosis pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis cystic fibrosis lung disease, modifier of cystic fibrosis CF |
|
IAO_0000115 |
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. |
|
IAO_0000233 | ||
id |
MONDO:0009061 |
|
inSubset |
http://purl.obolibrary.org/obo/mondo#ordo_disease http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#nord_rare |
|
label |
cystic fibrosis |
|
notation |
MONDO:0009061 |
|
prefLabel |
cystic fibrosis |
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seeAlso |
https://rarediseases.info.nih.gov/diseases/6233/cystic-fibrosis |
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excluded_subClassOf |
http://purl.obolibrary.org/obo/MONDO_0015509 http://purl.obolibrary.org/obo/MONDO_0002356 |
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subClassOf |