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 |
---|---|---|---|---|---|
C0268225 | Aspartylglucosaminuria | AGA | 175 | aspartylglucosaminidase | P20933 |
C0019196 | Hepatitis C | AGA | 175 | aspartylglucosaminidase | P20933 |
C0162311 | Androgenetic Alopecia | AGA | 175 | aspartylglucosaminidase | P20933 |
C0699791 | Stomach Carcinoma | AGA | 175 | aspartylglucosaminidase | P20933 |
C0008325 | Cholecystitis | AGA | 175 | aspartylglucosaminidase | P20933 |
C0085207 | Gestational Diabetes | AGA | 175 | aspartylglucosaminidase | P20933 |
C0022104 | Irritable Bowel Syndrome | AGA | 175 | aspartylglucosaminidase | P20933 |
C0036341 | Schizophrenia | AGA | 175 | aspartylglucosaminidase | P20933 |
C0524620 | Metabolic Syndrome X | AGA | 175 | aspartylglucosaminidase | P20933 |
C0019294 | Hernia, Inguinal | AGA | 175 | aspartylglucosaminidase | P20933 |
C0011847 | Diabetes | AGA | 175 | aspartylglucosaminidase | P20933 |
C0007570 | Celiac Disease | AGA | 175 | aspartylglucosaminidase | P20933 |
C0038018 | Spondylolysis | AGA | 175 | aspartylglucosaminidase | P20933 |
C0016202 | Flatfoot | AGA | 175 | aspartylglucosaminidase | P20933 |
C0040128 | Thyroid Diseases | AGA | 175 | aspartylglucosaminidase | P20933 |
C0235946 | Cerebral atrophy | AGA | 175 | aspartylglucosaminidase | P20933 |
C2931840 | Aspartylglucosamidase (AGA) deficiency | AGA | 175 | aspartylglucosaminidase | P20933 |
C0024623 | Malignant neoplasm of stomach | AGA | 175 | aspartylglucosaminidase | P20933 |
C2239176 | Liver carcinoma | AGA | 175 | aspartylglucosaminidase | P20933 |
C4083212 | Alopecia, Male Pattern | AGA | 175 | aspartylglucosaminidase | P20933 |
C0026769 | Multiple Sclerosis | AGA | 175 | aspartylglucosaminidase | P20933 |
C0013336 | Dwarfism | AGA | 175 | aspartylglucosaminidase | P20933 |
C0282577 | Congenital Disorders of Glycosylation | AGA | 175 | aspartylglucosaminidase | P20933 |
C1321756 | Achalasia | AGA | 175 | aspartylglucosaminidase | P20933 |
C0023890 | Liver Cirrhosis | AGA | 175 | aspartylglucosaminidase | P20933 |
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Last updated: August 19, 2024