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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name | Gene Symbol | Gene ID ▲ | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0002395 | Alzheimer's Disease | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0018802 | Congestive heart failure | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0029456 | Osteoporosis | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0003872 | Arthritis, Psoriatic | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0376358 | Malignant neoplasm of prostate | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0014070 | Encephalomyelitis | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0011847 | Diabetes | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0220710 | Medium-chain acyl-coenzyme A dehydrogenase deficiency | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0220756 | Niemann-Pick Disease, Type C | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0020456 | Hyperglycemia | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C2931822 | Nasopharyngeal carcinoma | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0241005 | Creatine phosphokinase serum increased | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0015934 | Fetal Growth Retardation | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0036572 | Seizures | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0524620 | Metabolic Syndrome X | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0021390 | Inflammatory Bowel Diseases | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C3887523 | Very long chain acyl-CoA dehydrogenase deficiency | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0878544 | Cardiomyopathies | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C1956346 | Coronary Artery Disease | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0233794 | Memory impairment | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0268634 | Disorder of fatty acid metabolism | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0206655 | Alveolar rhabdomyosarcoma | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C3888391 | Nonnuclear polymorphic congenital cataract | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
| C0268596 | Multiple Acyl Coenzyme A Dehydrogenase Deficiency | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
