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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 |
|---|---|---|---|---|---|
| C0268263 | Multiple Sulfatase Deficiency Disease | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0026703 | Mucopolysaccharidoses | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0006826 | Malignant Neoplasms | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0406775 | Symmetrical dyschromatosis of extremities | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0023890 | Liver Cirrhosis | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C3463824 | MYELODYSPLASTIC SYNDROME | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0700095 | Central neuroblastoma | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0023891 | Liver Cirrhosis, Alcoholic | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0027819 | Neuroblastoma | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0026705 | Mucopolysaccharidosis II | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C1332977 | Childhood Leukemia | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C3875321 | Inflammatory dermatosis | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0023418 | leukemia | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0023895 | Liver diseases | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0018818 | Ventricular Septal Defects | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0028860 | Oculocerebrorenal Syndrome | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0011603 | Dermatitis | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0019693 | HIV Infections | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0008445 | Chondrodysplasia Punctata | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
| C0003467 | Anxiety | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0036341 | Schizophrenia | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0026703 | Mucopolysaccharidoses | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0033578 | Prostatic Neoplasms | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0376358 | Malignant neoplasm of prostate | ARSG | 22901 | arylsulfatase G | Q96EG1 |
