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
Displaying entries 12026 - 12050 of 62743 in total
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