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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 |
|---|---|---|---|---|---|
| C0020758 | Congenital ichthyosis | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0004096 | Asthma | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0033687 | Proteinuria | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0013604 | Edema | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0029443 | Osteomyelitis | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0029464 | Osteosclerosis | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0600139 | Prostate carcinoma | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0268731 | Renal glomerular disease | LPIN2 | 9663 | lipin 2 | Q92539 |
| C3875321 | Inflammatory dermatosis | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0410422 | Chronic multifocal osteomyelitis | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0021831 | Intestinal Diseases | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0027947 | Neutropenia | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0702166 | Acne | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0263859 | Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0268238 | Triglyceride storage disease with ichthyosis | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0020757 | Ichthyoses | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0031069 | Familial Mediterranean Fever | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0027651 | Neoplasms | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0231528 | Myalgia | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0023787 | Lipodystrophy | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0376358 | Malignant neoplasm of prostate | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0085576 | Iron-Refractory Iron Deficiency Anemia | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0026848 | Myopathy | LPIN2 | 9663 | lipin 2 | Q92539 |
| C1275685 | Avellino corneal dystrophy | LPIN2 | 9663 | lipin 2 | Q92539 |
| C0024523 | Malabsorption Syndrome | LPIN2 | 9663 | lipin 2 | Q92539 |
