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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 |
|---|---|---|---|---|---|
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0740457 | Malignant neoplasm of kidney | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0002878 | Anemia, Hemolytic | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0007134 | Renal Cell Carcinoma | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0006826 | Malignant Neoplasms | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| 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 |
| C0027092 | Myopia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0342482 | X-linked Adrenal Hypoplasia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0020758 | Congenital ichthyosis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0029422 | Osteochondrodysplasias | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C3714756 | Intellectual Disability | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0085636 | Photophobia | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0042109 | Urticaria | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0242383 | Age related macular degeneration | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0007131 | Non-Small Cell Lung Carcinoma | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0011644 | Scleroderma | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| 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 |
