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 |
---|---|---|---|---|---|
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 |
C0013395 | Dyspepsia | AGA | 175 | aspartylglucosaminidase | P20933 |
C0041671 | Attention Deficit Disorder | AGA | 175 | aspartylglucosaminidase | P20933 |
C0011991 | Diarrhea | AGA | 175 | aspartylglucosaminidase | P20933 |
C0027947 | Neutropenia | AGA | 175 | aspartylglucosaminidase | P20933 |
C0002170 | Alopecia | AGA | 175 | aspartylglucosaminidase | P20933 |
C1263846 | Attention deficit hyperactivity disorder | AGA | 175 | aspartylglucosaminidase | P20933 |
C0279671 | Cervical Squamous Cell Carcinoma | AGA | 175 | aspartylglucosaminidase | P20933 |
C0271441 | Chronic otitis media | AGA | 175 | aspartylglucosaminidase | P20933 |
C0024523 | Malabsorption Syndrome | AGA | 175 | aspartylglucosaminidase | P20933 |
C0041324 | Tuberculosis, Osteoarticular | AGA | 175 | aspartylglucosaminidase | P20933 |
C0011608 | Dermatitis Herpetiformis | AGA | 175 | aspartylglucosaminidase | P20933 |
C0038016 | Spondylolisthesis | AGA | 175 | aspartylglucosaminidase | P20933 |
C0343641 | Human papilloma virus infection | AGA | 175 | aspartylglucosaminidase | P20933 |
C0013080 | Down Syndrome | AGA | 175 | aspartylglucosaminidase | P20933 |
C0162819 | Skin Diseases, Vascular | AGA | 175 | aspartylglucosaminidase | P20933 |
C0036439 | Scoliosis, unspecified | AGA | 175 | aspartylglucosaminidase | P20933 |
C0014848 | Esophageal Achalasia | AGA | 175 | aspartylglucosaminidase | P20933 |
C0011849 | Diabetes Mellitus | AGA | 175 | aspartylglucosaminidase | P20933 |
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Last updated: August 19, 2024