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 ▼ |
---|---|---|---|---|---|
C0400966 | Non-alcoholic Fatty Liver Disease | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
C0020676 | Hypothyroidism | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
C0004114 | Astrocytoma | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
C0004509 | Azoospermia | HJV | 148738 | hemojuvelin BMP co-receptor | Q6ZVN8 |
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 |
C0002395 | Alzheimer's Disease | PNPLA7 | 375775 | patatin like phospholipase domain containing 7 | Q6ZV29 |
C0023434 | Chronic Lymphocytic Leukemia | CLEC17A | 388512 | C-type lectin domain containing 17A | Q6ZS10 |
C1862941 | Amyotrophic Lateral Sclerosis, Sporadic | OTOG | 340990 | otogelin | Q6ZRI0 |
C3554163 | DEAFNESS, AUTOSOMAL RECESSIVE 18B | OTOG | 340990 | otogelin | Q6ZRI0 |
C1384666 | hearing impairment | OTOG | 340990 | otogelin | Q6ZRI0 |
C0011053 | Deafness | OTOG | 340990 | otogelin | Q6ZRI0 |
C1862939 | AMYOTROPHIC LATERAL SCLEROSIS 1 | OTOG | 340990 | otogelin | Q6ZRI0 |
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Last updated: August 19, 2024