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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 |
|---|---|---|---|---|---|
| C0014070 | Encephalomyelitis | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0003850 | Arteriosclerosis | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0019196 | Hepatitis C | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0011847 | Diabetes | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0020445 | Hypercholesterolemia, Familial | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0276289 | Zika Virus Infection | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0278878 | Adult Glioblastoma | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0007682 | CNS disorder | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0034494 | Rabies (disorder) | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0034067 | Pulmonary Emphysema | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C1332977 | Childhood Leukemia | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C1621958 | Glioblastoma Multiforme | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0494463 | Alzheimer Disease, Late Onset | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0025958 | Microcephaly | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
| C0152013 | Adenocarcinoma of lung (disorder) | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C0024623 | Malignant neoplasm of stomach | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C3714756 | Intellectual Disability | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C0029408 | Degenerative polyarthritis | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C0027092 | Myopia | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C1800706 | Idiopathic Pulmonary Fibrosis | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C0699791 | Stomach Carcinoma | HS6ST2 | 90161 | heparan sulfate 6-O-sulfotransferase 2 | Q96MM7 |
| C0023467 | Leukemia, Myelocytic, Acute | GLB1L2 | 89944 | galactosidase beta 1 like 2 | Q8IW92 |
| C0342751 | Generalized glycogen storage disease of infants | STBD1 | 8987 | starch binding domain 1 | O95210 |
| C0017921 | Glycogen storage disease type II | STBD1 | 8987 | starch binding domain 1 | O95210 |
| C0030567 | Parkinson Disease | STBD1 | 8987 | starch binding domain 1 | O95210 |
