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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 ▲ |
|---|---|---|---|---|---|
| C0023895 | Liver diseases | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0003873 | Rheumatoid Arthritis | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0004030 | Aspergillosis | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0021390 | Inflammatory Bowel Diseases | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C2931822 | Nasopharyngeal carcinoma | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0027651 | Neoplasms | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0085207 | Gestational Diabetes | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0024138 | Lupus Erythematosus, Discoid | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0008055 | Chikungunya Fever | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0006826 | Malignant Neoplasms | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0004943 | Behcet Syndrome | CD209 | 30835 | CD209 molecule | Q9NNX6 |
| C0011633 | Dermatomyositis | IL1RAPL2 | 26280 | interleukin 1 receptor accessory protein like 2 | Q9NP60 |
| C1136249 | Mental Retardation, X-Linked | IL1RAPL2 | 26280 | interleukin 1 receptor accessory protein like 2 | Q9NP60 |
| C0004352 | Autistic Disorder | IL1RAPL2 | 26280 | interleukin 1 receptor accessory protein like 2 | Q9NP60 |
| C0006142 | Malignant neoplasm of breast | IL1RAPL2 | 26280 | interleukin 1 receptor accessory protein like 2 | Q9NP60 |
| C0027121 | Myositis | IL1RAPL2 | 26280 | interleukin 1 receptor accessory protein like 2 | Q9NP60 |
| C1510586 | Autism Spectrum Disorders | IL1RAPL2 | 26280 | interleukin 1 receptor accessory protein like 2 | Q9NP60 |
| C0019196 | Hepatitis C | IL1RAPL2 | 26280 | interleukin 1 receptor accessory protein like 2 | Q9NP60 |
| C0221356 | Brachycephaly | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
| C0086237 | Epilepsy, Cryptogenic | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
| C3550904 | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36 | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
| C0036857 | Severe intellectual disability | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
| C0029124 | Optic Atrophy | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
| C3714756 | Intellectual Disability | ALG13 | 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | Q9NP73 |
