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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 |
|---|---|---|---|---|---|
| C1704436 | Peripheral Arterial Diseases | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0751122 | Infantile Severe Myoclonic Epilepsy | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0023434 | Chronic Lymphocytic Leukemia | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0242350 | Erectile dysfunction | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0013595 | Eczema | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C4554007 | Uveoretinal Coloboma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0036572 | Seizures | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0014544 | Epilepsy | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0029456 | Osteoporosis | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C1839333 | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C3203102 | Idiopathic pulmonary arterial hypertension | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0549622 | Sexual Dysfunction | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0015930 | Fetal Distress | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C3714756 | Intellectual Disability | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C1306459 | Primary malignant neoplasm | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0006826 | Malignant Neoplasms | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0011615 | Dermatitis, Atopic | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0004096 | Asthma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0019196 | Hepatitis C | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C3714636 | Pneumonitis | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0271829 | Pendred's syndrome | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0600139 | Prostate carcinoma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0020630 | Hypophosphatasia | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C2931835 | Hyperprolinemia type 2 | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
| C0038379 | Strabismus | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
