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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 ▲ |
|---|---|---|---|---|---|
| C0085762 | Alcohol abuse | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C1306459 | Primary malignant neoplasm | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0036341 | Schizophrenia | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0023895 | Liver diseases | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0546837 | Malignant neoplasm of esophagus | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0376670 | Pancreatitis, Alcoholic | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0009402 | Colorectal Carcinoma | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0279626 | Squamous cell carcinoma of esophagus | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0002395 | Alzheimer's Disease | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0018798 | Congenital Heart Defects | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0271650 | Impaired glucose tolerance | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0023530 | Leukopenia | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0007222 | Cardiovascular Diseases | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0011884 | Diabetic Retinopathy | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0004096 | Asthma | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0004352 | Autistic Disorder | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0853193 | Bipolar I disorder | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0000768 | Congenital Abnormality | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0010054 | Coronary Arteriosclerosis | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0520459 | Necrotizing Enterocolitis | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0751295 | Memory Loss | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0699791 | Stomach Carcinoma | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0011570 | Mental Depression | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0152021 | Congenital heart disease | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0010068 | Coronary heart disease | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
