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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 |
|---|---|---|---|---|---|
| C0162566 | Porphyria Cutanea Tarda | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0003811 | Cardiac Arrhythmia | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0002875 | Cooley's anemia | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0162429 | Malnutrition | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C3463824 | MYELODYSPLASTIC SYNDROME | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0085580 | Essential Hypertension | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0242350 | Erectile dysfunction | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0149782 | Squamous cell carcinoma of lung | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0038454 | Cerebrovascular accident | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0740391 | Middle Cerebral Artery Occlusion | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C3665349 | Secondary hypothyroidism | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0006142 | Malignant neoplasm of breast | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0271623 | Hypogonadotropic hypogonadism | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0268059 | Neonatal hemochromatosis | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
| C0024117 | Chronic Obstructive Airway Disease | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0005122 | Beriberi | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0020538 | Hypertensive disease | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0023467 | Leukemia, Myelocytic, Acute | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0007766 | Intracranial Aneurysm | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0039841 | Thiamine Deficiency | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0008354 | Cholera | CTBS | 1486 | chitobiase | Q01459 |
| C0003850 | Arteriosclerosis | CTBS | 1486 | chitobiase | Q01459 |
| C0376358 | Malignant neoplasm of prostate | CTBS | 1486 | chitobiase | Q01459 |
| C0002736 | Amyotrophic Lateral Sclerosis | CTBS | 1486 | chitobiase | Q01459 |
| C0027651 | Neoplasms | CTBS | 1486 | chitobiase | Q01459 |
