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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
idiopathic pulmonary fibrosis
Summary
- Synonym
-
- FIBROCYSTIC PULMONARY DYSPLASIA
- IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
- cryptogenic fibrosing alveolitis
- Definition
- A pulmonary fibrosis that is characterized by scarring of the lung.
- Super Class
- pulmonary fibrosis
External Links
- Disease Ontology
- DOID:0050156
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 90161 | HS6ST2 | heparan sulfate 6-O-sulfotransferase 2 | |
| 253558 | LCLAT1 | lysocardiolipin acyltransferase 1 | |
| 653509 | SFTPA1 | surfactant protein A1 | |
| 729238 | SFTPA2 | surfactant protein A2 | |
| 100507436 | MICA | MHC class I polypeptide-related sequence A |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002875 | Exertional dyspnea |
| HP:0100759 | Clubbing of fingers |
| HP:0002110 | Bronchiectasis |
| HP:0012378 | Fatigue |
| HP:0002020 | Gastroesophageal reflux |
| HP:0006530 | Abnormal pulmonary interstitial morphology |
| HP:0012735 | Cough |
| HP:0002206 | Pulmonary fibrosis |
| HP:0001063 | Acrocyanosis |
| HP:0010444 | Pulmonary insufficiency |
