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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 |
|---|---|---|---|---|---|
| C0027651 | Neoplasms | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0400966 | Non-alcoholic Fatty Liver Disease | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0041696 | Unipolar Depression | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0034194 | Pyloric Stenosis | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0023269 | leiomyosarcoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C1306459 | Primary malignant neoplasm | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0033687 | Proteinuria | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0009402 | Colorectal Carcinoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0036341 | Schizophrenia | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C3714756 | Intellectual Disability | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0268731 | Renal glomerular disease | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C1136249 | Mental Retardation, X-Linked | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0016202 | Flatfoot | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0011570 | Mental Depression | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C2239176 | Liver carcinoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0038379 | Strabismus | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0027868 | Neuromuscular Diseases | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0027092 | Myopia | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C1261473 | Sarcoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C1845672 | Mental Retardation, X-Linked 63 | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0235991 | Small for gestational age (disorder) | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0699791 | Stomach Carcinoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0006826 | Malignant Neoplasms | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0678222 | Breast Carcinoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C1567741 | Alport Syndrome | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
