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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 |
|---|---|---|---|---|---|
| C1412036 | Anal squamous cell carcinoma | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0027051 | Myocardial Infarction | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0398623 | Thrombophilia | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0338106 | Adenocarcinoma of colon | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0026769 | Multiple Sclerosis | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C4551506 | Paroxysmal Nonkinesigenic Dyskinesia 1 | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C1328479 | Pancreatic Endocrine Carcinoma | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C1333990 | Hereditary Nonpolyposis Colorectal Cancer | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C1621958 | Glioblastoma Multiforme | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0497327 | Dementia | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0751688 | Malignant Squamous Cell Neoplasm | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0018021 | Goiter | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0005695 | Bladder Neoplasm | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0013146 | Drug abuse | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0005684 | Malignant neoplasm of urinary bladder | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0566602 | Primary sclerosing cholangitis | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C0027877 | Neuronal Ceroid-Lipofuscinoses | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0751783 | Lafora Disease | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C1850442 | CEROID LIPOFUSCINOSIS, NEURONAL, 5 | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C1838571 | Ceroid Lipofuscinosis, Neuronal, 7 | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0235946 | Cerebral atrophy | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0022340 | Late-Infantile Neuronal Ceroid Lipfuscinosis | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C1864923 | Northern epilepsy syndrome | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0751383 | Juvenile Neuronal Ceroid Lipofuscinosis | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
