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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 |
|---|---|---|---|---|---|
| C0027868 | Neuromuscular Diseases | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0011581 | Depressive disorder | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0004106 | Astigmatism | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0022541 | Kearns-Sayre syndrome | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0011570 | Mental Depression | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0149940 | Sciatic Neuropathy | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0162309 | Adrenoleukodystrophy | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0010068 | Coronary heart disease | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0206733 | Strawberry nevus of skin | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0152025 | Polyneuropathy | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C3714756 | Intellectual Disability | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0004936 | Mental disorders | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C1306459 | Primary malignant neoplasm | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C1857276 | Trichohepatoenteric Syndrome | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C1269683 | Major Depressive Disorder | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0270911 | Charcot-Marie-Tooth Disease, Type Ia (disorder) | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0027651 | Neoplasms | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0242422 | Parkinsonian Disorders | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C2750737 | DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0740391 | Middle Cerebral Artery Occlusion | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0015934 | Fetal Growth Retardation | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0002726 | Amyloidosis | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0037773 | Spastic Paraplegia, Hereditary | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0017638 | Glioma | MAG | 4099 | myelin associated glycoprotein | P20916 |
| C0000768 | Congenital Abnormality | MAG | 4099 | myelin associated glycoprotein | P20916 |
