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 |
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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. |
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ID |
http://purl.obolibrary.org/obo/MONDO_0009061 |
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alternative label |
mucoviscidosis pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis cystic fibrosis lung disease, modifier of cystic fibrosis CF |
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has exact synonym |
mucoviscidosis pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis cystic fibrosis lung disease, modifier of cystic fibrosis CF |
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hasDbXref |
ICD10CM:E84 Orphanet:586 OMIM:219700 UMLS:C0010674 SCTID:190905008 MESH:D003550 GARD:0006233 MedDRA:10011762 DOID:1485 ICD9:277.0 NCIT:C2975 |
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imported from | ||
inSubset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#rare http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_disease http://purl.oboInOwllibrary.org/oboInOwl/mondo#gard_rare http://purl.oboInOwllibrary.org/oboInOwl/mondo#mondo_rare http://purl.oboInOwllibrary.org/oboInOwl/mondo#orphanet_rare |
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label |
cystic fibrosis |
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prefixIRI |
MONDO:0009061 |
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prefLabel |
cystic fibrosis |
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textual 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. |
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subClassOf |