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BioAssay Ontology
Last uploaded:
January 17, 2025
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| Id | http://purl.obolibrary.org/obo/DOID_0050156
http://purl.obolibrary.org/obo/DOID_0050156
|
|---|---|
| Preferred Name | idiopathic pulmonary fibrosis |
| Definitions |
A pulmonary fibrosis that is characterized by scarring of the lung.
OMIM mapping confirmed by DO. [SN].
|
| Synonyms |
FIBROCYSTIC PULMONARY DYSPLASIA
IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
cryptogenic fibrosing alveolitis
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label |
idiopathic pulmonary fibrosis
|
|---|---|
| comment |
OMIM mapping confirmed by DO. [SN].
|
| prefLabel |
idiopathic pulmonary fibrosis
|
| has cross-reference |
ICD9CM:516.31
SNOMEDCT_US_2020_03_01:28168000
ICD10CM:J84.112
UMLS_CUI:C1800706
MESH:D054990
OMIM:178500
EFO:0000768
GARD:8609
NCI:C35716
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|
| notation |
DOID:0050156
|
| in_subset | |
| id |
DOID:0050156
|
| has_obo_namespace |
disease_ontology
|
| textual definition |
A pulmonary fibrosis that is characterized by scarring of the lung.
|
| subClassOf | |
| imported from | |
| type | |
| has exact synonym |
FIBROCYSTIC PULMONARY DYSPLASIA
IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
cryptogenic fibrosing alveolitis
|
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