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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 |
|---|---|---|---|---|---|
| C0687120 | Nephronophthisis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0022578 | Keratoconus | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0027765 | nervous system disorder | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0020258 | Hydrocephalus, Normal Pressure | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0011351 | Dental Enamel Hypoplasia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0036439 | Scoliosis, unspecified | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0079583 | Ichthyosiform Erythroderma, Congenital | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0036572 | Seizures | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0025958 | Microcephaly | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0041834 | Erythema | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0034372 | Quadriplegia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0013336 | Dwarfism | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0023882 | Little's Disease | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0036421 | Systemic Scleroderma | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0023772 | Lipid Metabolism, Inborn Errors | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0035309 | Retinal Diseases | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C1865349 | Ethylmalonic encephalopathy | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0019163 | Hepatitis B | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0025362 | Mental Retardation | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0220766 | Congenital hypoplasia of adrenal gland | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0011603 | Dermatitis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0543874 | Apraxia, oculomotor, Cogan type | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0205875 | Papillomatosis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0403553 | Renal dysplasia and retinal aplasia (disorder) | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
