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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 |
|---|---|---|---|---|---|
| C0021390 | Inflammatory Bowel Diseases | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C3665347 | Visual Impairment | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C3463824 | MYELODYSPLASTIC SYNDROME | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0041341 | Tuberous Sclerosis | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1704356 | Enchondroma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0079744 | Diffuse Large B-Cell Lymphoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0008479 | Chondrosarcoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0085110 | Severe Combined Immunodeficiency | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0279628 | Adenocarcinoma Of Esophagus | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0011195 | Dejerine-Sottas Disease (disorder) | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0238463 | Papillary thyroid carcinoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0149931 | Migraine Disorders | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0268398 | Familial lichen amyloidosis | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0024894 | Mastitis | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0041696 | Unipolar Depression | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0041296 | Tuberculosis | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0019621 | Histiocytosis, Langerhans-Cell | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0086565 | Liver Dysfunction | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0038454 | Cerebrovascular accident | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0026691 | Mucocutaneous Lymph Node Syndrome | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1266044 | Collecting Duct Carcinoma of the Kidney | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0522631 | Acute myeloid leukemia, minimal differentiation | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0282528 | Peroxisomal Disorders | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0009404 | Colorectal Neoplasms | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0238339 | Hereditary pancreatitis | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
