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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0023434 | Chronic Lymphocytic Leukemia | ARSH | 347527 | arylsulfatase family member H | Q5FYA8 |
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 |
C0004153 | Atherosclerosis | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
C0003467 | Anxiety | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
C0004352 | Autistic Disorder | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
C1279420 | Anxiety neurosis (finding) | ARSI | 340075 | arylsulfatase family member I | Q5FYB1 |
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Last updated: August 19, 2024