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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 |
|---|---|---|---|---|---|
| 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 |
| C0027819 | Neuroblastoma | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C4721532 | Lymphoma, Non-Hodgkin, Familial | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0175707 | Asplenia Syndrome | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3536741 | Discordant ventriculoarterial connection | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1415817 | HETEROTAXY, VISCERAL, 2, AUTOSOMAL | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0700095 | Central neuroblastoma | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3178805 | Heterotaxy Syndrome | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3178806 | Right Atrial Isomerism | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0040761 | Transposition of Great Vessels | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0010068 | Coronary heart disease | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1970109 | AROMATASE EXCESS SYNDROME | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0023895 | Liver diseases | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1389016 | ATRIOVENTRICULAR CANAL DEFECT | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0520463 | Chronic active hepatitis | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0265357 | Polysplenia Syndrome | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
