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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 |
|---|---|---|---|---|---|
| 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 |
| C0027651 | Neoplasms | AGA | 175 | aspartylglucosaminidase | P20933 |
| C0021400 | Influenza | AGA | 175 | aspartylglucosaminidase | P20933 |
| C1832648 | Hypoparathyroidism familial isolated | AGA | 175 | aspartylglucosaminidase | P20933 |
| C0011334 | Dental caries | AGA | 175 | aspartylglucosaminidase | P20933 |
| C0376480 | Gingival Overgrowth | AGA | 175 | aspartylglucosaminidase | P20933 |
| C0004031 | Aspergillosis, Allergic Bronchopulmonary | AGA | 175 | aspartylglucosaminidase | P20933 |
| C1306503 | Congenital exomphalos | AGA | 175 | aspartylglucosaminidase | P20933 |
| C0002986 | Fabry Disease | AGA | 175 | aspartylglucosaminidase | P20933 |
| C1864172 | Peroxisome Biogenesis Disorder, Complementation Group G | AGA | 175 | aspartylglucosaminidase | P20933 |
| C0015934 | Fetal Growth Retardation | AGA | 175 | aspartylglucosaminidase | P20933 |
| C0156173 | Functional diarrhea | AGA | 175 | aspartylglucosaminidase | P20933 |
| C4049006 | Selective immunoglobulin A deficiency | AGA | 175 | aspartylglucosaminidase | P20933 |
