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loading...| Preferred Name |
cystic fibrosis |
| Synonyms |
mucoviscidosis CF |
| Definitions |
An autosomal recessive disease that is characterized by the buildup of thick, sticky mucus that can damage many organs. OMIM mapping confirmed by DO. [SN]. |
| ID |
http://purl.obolibrary.org/obo/DOID_1485 |
| comment |
OMIM mapping confirmed by DO. [SN]. |
| database_cross_reference |
SNOMEDCT_US_2016_03_01:190911006 SNOMEDCT_US_2016_03_01:190905008 ICD10CM:E84 ICD9CM:277.0 SNOMEDCT_US_2016_03_01:154767009 MESH:D003550 OMIM:219700 NCI:C2975 ICD10CM:E84.9 SNOMEDCT_US_2016_03_01:85809002 UMLS_CUI:C0010674 |
| has exact synonym |
mucoviscidosis CF |
| has_alternative_id |
DOID:13383 DOID:14395 DOID:1484 DOID:12447 |
| has_obo_namespace |
disease_ontology |
| id |
DOID:1485 |
| imported from | |
| label |
cystic fibrosis |
| notation |
DOID:1485 |
| prefLabel |
cystic fibrosis |
| textual definition |
An autosomal recessive disease that is characterized by the buildup of thick, sticky mucus that can damage many organs. |
| subClassOf |
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