Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
|---|---|---|---|---|---|
| C0268263 | Multiple Sulfatase Deficiency Disease | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0011880 | Diabetic Ketoacidosis | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0019572 | Hirsutism | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0014518 | Toxic Epidermal Necrolysis | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0028738 | Nystagmus | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0011991 | Diarrhea | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0270707 | Kluver-Bucy Syndrome | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C4048196 | beta-Mannosidosis | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0205700 | Asymmetric Septal Hypertrophy | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0086649 | MPS III C | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0036572 | Seizures | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0003125 | Anorexia Nervosa | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C2931845 | Neurodegeneration with brain iron accumulation (NBIA) | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0038013 | Ankylosing spondylitis | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0007682 | CNS disorder | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0009324 | Ulcerative Colitis | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0009402 | Colorectal Carcinoma | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0017638 | Glioma | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0019196 | Hepatitis C | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0007097 | Carcinoma | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0017636 | Glioblastoma | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C2239176 | Liver carcinoma | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C1621958 | Glioblastoma Multiforme | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0279628 | Adenocarcinoma Of Esophagus | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0022283 | Incontinentia Pigmenti Achromians | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
