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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 |
|---|---|---|---|---|---|
| C0442874 | Neuropathy | ENO2 | 2026 | enolase 2 | P09104 |
| C0019337 | Heroin Dependence | ENO2 | 2026 | enolase 2 | P09104 |
| C0231528 | Myalgia | ENO3 | 2027 | enolase 3 | P13929 |
| C0004364 | Autoimmune Diseases | ENO3 | 2027 | enolase 3 | P13929 |
| C0242379 | Malignant neoplasm of lung | ENO3 | 2027 | enolase 3 | P13929 |
| C0086565 | Liver Dysfunction | ENO3 | 2027 | enolase 3 | P13929 |
| C0031099 | Periodontitis | ENO3 | 2027 | enolase 3 | P13929 |
| C0155567 | Rheumatic aortic stenosis | ENO3 | 2027 | enolase 3 | P13929 |
| C0003507 | Aortic Valve Stenosis | ENO3 | 2027 | enolase 3 | P13929 |
| C0152417 | Congenital stenosis of aortic valve | ENO3 | 2027 | enolase 3 | P13929 |
| C0025517 | Metabolic Diseases | ENO3 | 2027 | enolase 3 | P13929 |
| C0017919 | Glycogen Storage Disease | ENO3 | 2027 | enolase 3 | P13929 |
| C0023895 | Liver diseases | ENO3 | 2027 | enolase 3 | P13929 |
| C0400966 | Non-alcoholic Fatty Liver Disease | ENO3 | 2027 | enolase 3 | P13929 |
| C0684249 | Carcinoma of lung | ENO3 | 2027 | enolase 3 | P13929 |
| C0020538 | Hypertensive disease | ENO3 | 2027 | enolase 3 | P13929 |
| C0241005 | Creatine phosphokinase serum increased | ENO3 | 2027 | enolase 3 | P13929 |
| C1265996 | Large cell neuroendocrine carcinoma | ENO3 | 2027 | enolase 3 | P13929 |
| C3554349 | ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9 | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0079154 | Congenital Nonbullous Ichthyosiform Erythroderma | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0020758 | Congenital ichthyosis | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0013336 | Dwarfism | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C1384666 | hearing impairment | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C4551675 | Keratoderma, Palmoplantar | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
| C0020620 | Hypohidrosis | CERS3 | 204219 | ceramide synthase 3 | Q8IU89 |
