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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 ▼ |
|---|---|---|---|---|---|
| C0007131 | Non-Small Cell Lung Carcinoma | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0376358 | Malignant neoplasm of prostate | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0006142 | Malignant neoplasm of breast | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0004096 | Asthma | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0235480 | Paroxysmal atrial fibrillation | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0268060 | Juvenile hemochromatosis | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0003873 | Rheumatoid Arthritis | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0009402 | Colorectal Carcinoma | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0007785 | Cerebral Infarction | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0740391 | Middle Cerebral Artery Occlusion | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0026769 | Multiple Sclerosis | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C2239176 | Liver carcinoma | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0006826 | Malignant Neoplasms | RGMB | 285704 | repulsive guidance molecule BMP co-receptor b | Q6NW40 |
| C0023264 | Leigh Disease | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0027066 | Myoclonus | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0039685 | Tetralogy of Fallot | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0029408 | Degenerative polyarthritis | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0524851 | Neurodegenerative Disorders | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0085584 | Encephalopathies | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0038379 | Strabismus | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0025521 | Inborn Errors of Metabolism | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0013421 | Dystonia | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0027651 | Neoplasms | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0010417 | Cryptorchidism | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0036572 | Seizures | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
