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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 |
|---|---|---|---|---|---|
| C1848745 | Oliver-McFarlane syndrome | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C2981150 | Uranostaphyloschisis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C1260873 | Aortic valve disorder | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0280324 | Laryngeal Squamous Cell Carcinoma | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0279651 | Gallbladder adenocarcinoma | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0085409 | Polyendocrinopathies, Autoimmune | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0003467 | Anxiety | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0750974 | Brain Tumor, Primary | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0085110 | Severe Combined Immunodeficiency | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0007103 | Malignant neoplasm of endometrium | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C1859726 | ARTERIAL TORTUOSITY SYNDROME | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0017152 | Gastritis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0020179 | Huntington Disease | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C2242813 | Ranula (disorder) | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0392607 | Severe combined immunodeficiency due to adenosine deaminase deficiency | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0031099 | Periodontitis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0013080 | Down Syndrome | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0014544 | Epilepsy | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0024959 | Maxillary Sinusitis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0026703 | Mucopolysaccharidoses | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0010054 | Coronary Arteriosclerosis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0024904 | Mastoiditis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0795864 | Smith-Magenis syndrome | NT5M | 56953 | 5',3'-nucleotidase, mitochondrial | Q9NPB1 |
| C3150878 | Primary hyperoxaluria type III | HOGA1 | 112817 | 4-hydroxy-2-oxoglutarate aldolase 1 | Q86XE5 |
| C0020501 | Primary Hyperoxaluria | HOGA1 | 112817 | 4-hydroxy-2-oxoglutarate aldolase 1 | Q86XE5 |
