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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 ▼ |
|---|---|---|---|---|---|
| C0011884 | Diabetic Retinopathy | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0013264 | Muscular Dystrophy, Duchenne | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0020538 | Hypertensive disease | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0015414 | Eye Neoplasms | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0019061 | Hemolytic-Uremic Syndrome | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0015934 | Fetal Growth Retardation | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0745103 | Hyperlipoproteinemia Type IIa | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0205851 | Germ cell tumor | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0004352 | Autistic Disorder | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0497327 | Dementia | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0678222 | Breast Carcinoma | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0002395 | Alzheimer's Disease | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0035335 | Retinoblastoma | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0220633 | Uveal melanoma | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0014175 | Endometriosis | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0026850 | Muscular Dystrophy | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
| C3809216 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14 | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
| C3809221 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14 | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
| C0018784 | Sensorineural Hearing Loss (disorder) | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
| C0520947 | Clumsiness - motor delay | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
| C0086543 | Cataract | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
| C0008925 | Cleft Palate | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
| C0026848 | Myopathy | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
| C1531647 | Cerebral ventriculomegaly | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
| C0686353 | Muscular Dystrophies, Limb-Girdle | GMPPB | 29925 | GDP-mannose pyrophosphorylase B | Q9Y5P6 |
