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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 ▼ |
|---|---|---|---|---|---|
| C0003850 | Arteriosclerosis | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0268228 | Neuraminidase 1 deficiency | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0023806 | Lipomucopolysaccharidosis | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0268226 | Type I Mucolipidosis | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0751776 | Atypical Inclusion-Body Disease | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C1956346 | Coronary Artery Disease | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C4721610 | Carcinoma, Ovarian Epithelial | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C1458155 | Mammary Neoplasms | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C1134719 | Invasive Ductal Breast Carcinoma | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C1140680 | Malignant neoplasm of ovary | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0007103 | Malignant neoplasm of endometrium | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0004997 | Benign Ovarian Neoplasm | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0751778 | Myoclonic Epilepsies, Progressive | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0029401 | Osteitis Deformans | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0476089 | Endometrial Carcinoma | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C1306459 | Primary malignant neoplasm | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0027651 | Neoplasms | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0024623 | Malignant neoplasm of stomach | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0086795 | Pfaundler-Hurler Syndrome | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0025362 | Mental Retardation | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C4282398 | Sialidase deficiency | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0085078 | Lysosomal Storage Diseases | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0010346 | Crohn Disease | NEU1 | 4758 | neuraminidase 1 | Q99519 |
| C0037822 | Speech Disorders | NEU1 | 4758 | neuraminidase 1 | Q99519 |
