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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 |
|---|---|---|---|
| 142 | PARP1 | poly(ADP-ribose) polymerase 1 | |
| 207 | AKT1 | AKT serine/threonine kinase 1 | |
| 240 | ALOX5 | arachidonate 5-lipoxygenase | |
| 248 | ALPI | alkaline phosphatase, intestinal | |
| 250 | ALPP | alkaline phosphatase, placental | |
| 308 | ANXA5 | annexin A5 | |
| 1048 | CEACAM5 | CEA cell adhesion molecule 5 | |
| 1056 | CEL | carboxyl ester lipase | |
| 1087 | CEACAM7 | CEA cell adhesion molecule 7 | |
| 1116 | CHI3L1 | chitinase 3 like 1 |
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 |
