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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 |
|---|---|---|---|---|---|
| C0270855 | Early myoclonic encephalopathy | AMT | 275 | aminomethyltransferase | P48728 |
| C0008533 | Hemophilia B | AMT | 275 | aminomethyltransferase | P48728 |
| C3714756 | Intellectual Disability | AMT | 275 | aminomethyltransferase | P48728 |
| C1510586 | Autism Spectrum Disorders | AMT | 275 | aminomethyltransferase | P48728 |
| C0022336 | Creutzfeldt-Jakob disease | AMT | 275 | aminomethyltransferase | P48728 |
| C0025517 | Metabolic Diseases | AMT | 275 | aminomethyltransferase | P48728 |
| C0026769 | Multiple Sclerosis | AMT | 275 | aminomethyltransferase | P48728 |
| C1306459 | Primary malignant neoplasm | AMT | 275 | aminomethyltransferase | P48728 |
| C0006826 | Malignant Neoplasms | AMT | 275 | aminomethyltransferase | P48728 |
| C0027651 | Neoplasms | AMT | 275 | aminomethyltransferase | P48728 |
| C0085584 | Encephalopathies | AMT | 275 | aminomethyltransferase | P48728 |
| C0699889 | Malignant Female Reproductive System Neoplasm | AMT | 275 | aminomethyltransferase | P48728 |
| C0023817 | Hyperlipoproteinemia Type I | AMT | 275 | aminomethyltransferase | P48728 |
| C0011581 | Depressive disorder | AMT | 275 | aminomethyltransferase | P48728 |
| C0009402 | Colorectal Carcinoma | AMT | 275 | aminomethyltransferase | P48728 |
| C0014544 | Epilepsy | AMT | 275 | aminomethyltransferase | P48728 |
| C0220994 | Hyperammonemia | AMT | 275 | aminomethyltransferase | P48728 |
| C0010346 | Crohn Disease | AMT | 275 | aminomethyltransferase | P48728 |
| C0009402 | Colorectal Carcinoma | AMDHD2 | 51005 | amidohydrolase domain containing 2 | Q9Y303 |
| C0007134 | Renal Cell Carcinoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0600139 | Prostate carcinoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0027651 | Neoplasms | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0376358 | Malignant neoplasm of prostate | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1858328 | Bile acid synthesis defect, congenital, 4 | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1704272 | Benign Prostatic Hyperplasia | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
