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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 |
|---|---|---|---|---|---|
| C0017924 | Glycogen Storage Disease Type V | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0025517 | Metabolic Diseases | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0020456 | Hyperglycemia | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0751651 | Mitochondrial Diseases | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0027051 | Myocardial Infarction | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0017921 | Glycogen storage disease type II | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0241005 | Creatine phosphokinase serum increased | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0003811 | Cardiac Arrhythmia | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0019158 | Hepatitis | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0268596 | Multiple Acyl Coenzyme A Dehydrogenase Deficiency | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0025958 | Microcephaly | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0015934 | Fetal Growth Retardation | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C3714581 | Multicystic Dysplastic Kidney | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0018802 | Congestive heart failure | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0014038 | Encephalitis | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0027849 | Neuroleptic Malignant Syndrome | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0016202 | Flatfoot | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C1263846 | Attention deficit hyperactivity disorder | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C1829703 | Carnitine palmitoyl transferase 1A deficiency | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0007193 | Cardiomyopathy, Dilated | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0011849 | Diabetes Mellitus | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C1531647 | Cerebral ventriculomegaly | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C0027080 | Myoglobinuria | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
| C3463824 | MYELODYSPLASTIC SYNDROME | CPT2 | 1376 | carnitine palmitoyltransferase 2 | P23786 |
