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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 |
|---|---|---|---|---|---|
| C0751606 | Adult Acute Lymphocytic Leukemia | CERS6 | 253782 | ceramide synthase 6 | Q6ZMG9 |
| C0751651 | Mitochondrial Diseases | CERS6 | 253782 | ceramide synthase 6 | Q6ZMG9 |
| C0013222 | Drug Use Disorders | CERS6 | 253782 | ceramide synthase 6 | Q6ZMG9 |
| C0014070 | Encephalomyelitis | CERS6 | 253782 | ceramide synthase 6 | Q6ZMG9 |
| C0023896 | Alcoholic Liver Diseases | CERS6 | 253782 | ceramide synthase 6 | Q6ZMG9 |
| C1961099 | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | CERS6 | 253782 | ceramide synthase 6 | Q6ZMG9 |
| C0009319 | Colitis | CERS6 | 253782 | ceramide synthase 6 | Q6ZMG9 |
| 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 |
| C1876172 | VAH, AUTOSOMAL RECESSIVE | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0018817 | Atrial Septal Defects | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0344692 | Isomerism of atrial appendages | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
