Idiopathic Pulmonary Fibrosis
Disease ID: disease_node_12012
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| Dbxref | EFO:0000768, GARD:8609, ICD10CM:J84.112, ICD9CM:516.31, MESH:D054990, NCI:C35716, SNOMEDCT_US_2023_03_01:28168000, UMLS_CUI:C1800706 |
|---|---|
| Subclassof | DOID_3770, DOID_0050736 |
| Data Source | DOID, MESH |
| Synonyms | FIBROCYSTIC PULMONARY DYSPLASIA, IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL, cryptogenic fibrosing alveolitis |
| Mesh Id | D054990 |
| Mesh Label | Idiopathic Pulmonary Fibrosis |
| Mesh Subclassof | D011658 |
| Doid Label | idiopathic pulmonary fibrosis |
| Doid Description | A pulmonary fibrosis that is characterized by scarring of the lung characterized by stiffness in the lungs and makes it difficult to breathe. OMIM mapping confirmed by DO. [SN]. |
| Has Material Basis In | GENO_0000147, HP_0006530 |
| Disease Node Id | disease_node_12012 |
| Doid Id | DOID_0050156 |
| Label | Idiopathic Pulmonary Fibrosis |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Pulmonary Fibrosis(ID:disease_node_6437) (Disease)