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 ▼ |
---|---|---|---|---|---|
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 |
C0004153 | Atherosclerosis | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0007137 | Squamous cell carcinoma | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0024623 | Malignant neoplasm of stomach | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0042373 | Vascular Diseases | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0236970 | Alcohol-Induced Disorders | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0023891 | Liver Cirrhosis, Alcoholic | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0020459 | Hyperinsulinism | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0018799 | Heart Diseases | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0014859 | Esophageal Neoplasms | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0023890 | Liver Cirrhosis | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0018801 | Heart failure | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C0400966 | Non-alcoholic Fatty Liver Disease | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
C3469521 | FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
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Last updated: August 19, 2024