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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 ▲ |
|---|---|---|---|---|---|
| C0086648 | MPS III B | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0026703 | Mucopolysaccharidoses | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0029408 | Degenerative polyarthritis | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0002395 | Alzheimer's Disease | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0854723 | Retinal Dystrophies | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0026650 | Movement Disorders | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0038013 | Ankylosing spondylitis | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0007682 | CNS disorder | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0036572 | Seizures | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0011991 | Diarrhea | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0026706 | Mucopolysaccharidosis III | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0014518 | Toxic Epidermal Necrolysis | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0270707 | Kluver-Bucy Syndrome | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C1285162 | Degenerative disorder | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0086647 | Mucopolysaccharidosis Type IIIA | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0268263 | Multiple Sulfatase Deficiency Disease | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0086795 | Pfaundler-Hurler Syndrome | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0022541 | Kearns-Sayre syndrome | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0035334 | Retinitis Pigmentosa | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0086650 | MPS III D | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0042571 | Vertigo | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0006826 | Malignant Neoplasms | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C1269683 | Major Depressive Disorder | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0085078 | Lysosomal Storage Diseases | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0011880 | Diabetic Ketoacidosis | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
