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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 |
|---|---|---|---|---|---|
| C0011581 | Depressive disorder | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0007131 | Non-Small Cell Lung Carcinoma | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0242379 | Malignant neoplasm of lung | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C1176475 | Ductal Carcinoma | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0684249 | Carcinoma of lung | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0006142 | Malignant neoplasm of breast | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0011269 | Dementia, Vascular | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C2239176 | Liver carcinoma | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0019196 | Hepatitis C | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0265252 | Coffin-Lowry syndrome | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0027708 | Nephroblastoma | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0036341 | Schizophrenia | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0016034 | Breast Fibrocystic Disease | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0281267 | bilateral breast cancer | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0024790 | Paroxysmal nocturnal hemoglobinuria | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C3495439 | Inflammatory disorder of breast | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0009451 | Communicating Hydrocephalus | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
| C0686353 | Muscular Dystrophies, Limb-Girdle | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
| C3553330 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7 | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
| C0026848 | Myopathy | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
| C4015095 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
| C0010038 | Corneal Opacity | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
| C0266544 | Microcornea | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
| C0020256 | Congenital Hydrocephalus | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | CRPPA | 729920 | CDP-L-ribitol pyrophosphorylase A | A4D126 |
