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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 |
|---|---|---|---|---|---|
| C0014548 | Epilepsy, Generalized | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0752206 | Dystonias, Sporadic | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C1140680 | Malignant neoplasm of ovary | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0036572 | Seizures | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0242383 | Age related macular degeneration | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0752203 | Dystonia, Primary | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0494475 | Tonic - clonic seizures | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0752202 | Childhood Onset Dystonias | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0003467 | Anxiety | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0038379 | Strabismus | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0007124 | Noninfiltrating Intraductal Carcinoma | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0010346 | Crohn Disease | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0036857 | Severe intellectual disability | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0035372 | Rett Syndrome | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0001973 | Alcoholic Intoxication, Chronic | ALDH3B2 | 222 | aldehyde dehydrogenase 3 family member B2 | P48448 |
| C0036341 | Schizophrenia | ALDH3B1 | 221 | aldehyde dehydrogenase 3 family member B1 | P43353 |
| C0036349 | Paranoid Schizophrenia | ALDH3B1 | 221 | aldehyde dehydrogenase 3 family member B1 | P43353 |
| C0007134 | Renal Cell Carcinoma | ALDH3B1 | 221 | aldehyde dehydrogenase 3 family member B1 | P43353 |
| C0004096 | Asthma | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0020757 | Ichthyoses | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0037231 | Sjogren-Larsson Syndrome | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0079154 | Congenital Nonbullous Ichthyosiform Erythroderma | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0870082 | Hyperkeratosis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0037772 | Spastic Paraplegia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0035334 | Retinitis Pigmentosa | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
