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