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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 |
|---|---|---|---|---|---|
| C1956413 | Taussig-Bing Anomaly | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0002395 | Alzheimer's Disease | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0152021 | Congenital heart disease | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0005411 | Biliary Atresia | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C4520983 | Congenital atresia of extrahepatic bile duct | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3151057 | HETEROTAXY, VISCERAL, 4, AUTOSOMAL | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0027651 | Neoplasms | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0024530 | Malaria | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C2910124 | Isomerism of atrial appendages with asplenia or polysplenia | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0006826 | Malignant Neoplasms | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1876171 | Polyasplenia | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0037221 | Situs Inversus | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1844020 | HETEROTAXY, VISCERAL, 1, X-LINKED | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1876173 | Heterotaxy, Visceroatrial, Autosomal Recessive | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1837341 | Transposition of the Great Arteries, Dextro-Looped 1 | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3257801 | Dextrotransposition of aorta | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0013069 | Double Outlet Right Ventricle | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1306459 | Primary malignant neoplasm | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C1853444 | Heterotaxy, Visceral, 3, Autosomal | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C2936858 | Congenital adrenal hyperplasia due to 21 hydroxylase deficiency | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0024305 | Lymphoma, Non-Hodgkin | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0025517 | Metabolic Diseases | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C0000768 | Congenital Abnormality | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3151867 | CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
| C3463824 | MYELODYSPLASTIC SYNDROME | CFC1 | 55997 | cripto, FRL-1, cryptic family 1 | P0CG37 |
