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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 |
|---|---|---|---|---|---|
| C0023015 | Language Disorders | ARSD | 414 | arylsulfatase D | P51689 |
| C1862389 | ATRIAL SEPTAL DEFECT 1 | ARSD | 414 | arylsulfatase D | P51689 |
| C0011570 | Mental Depression | ARSD | 414 | arylsulfatase D | P51689 |
| C0011581 | Depressive disorder | ARSD | 414 | arylsulfatase D | P51689 |
| C0848558 | Hypospadias | ARSD | 414 | arylsulfatase D | P51689 |
| C0025362 | Mental Retardation | ARSD | 414 | arylsulfatase D | P51689 |
| C0004936 | Mental disorders | ARSD | 414 | arylsulfatase D | P51689 |
| C0013473 | Eating Disorders | ARSD | 414 | arylsulfatase D | P51689 |
| C0004245 | Atrioventricular Block | ARSD | 414 | arylsulfatase D | P51689 |
| C0175702 | Williams Syndrome | ARSD | 414 | arylsulfatase D | P51689 |
| C1263846 | Attention deficit hyperactivity disorder | ARSD | 414 | arylsulfatase D | P51689 |
| C0016522 | Foramen Ovale, Patent | ARSD | 414 | arylsulfatase D | P51689 |
| C0014175 | Endometriosis | ARSD | 414 | arylsulfatase D | P51689 |
| C0018553 | Hamartoma Syndrome, Multiple | ARSD | 414 | arylsulfatase D | P51689 |
| C1409792 | Coronary sinus defect | ARSD | 414 | arylsulfatase D | P51689 |
| C0023487 | Acute Promyelocytic Leukemia | ARSD | 414 | arylsulfatase D | P51689 |
| C0018818 | Ventricular Septal Defects | ARSD | 414 | arylsulfatase D | P51689 |
| C0010068 | Coronary heart disease | ARSD | 414 | arylsulfatase D | P51689 |
| C0026010 | Microphthalmos | ARSD | 414 | arylsulfatase D | P51689 |
| C0034089 | Pulmonary Valve Stenosis | ARSD | 414 | arylsulfatase D | P51689 |
| C0007789 | Cerebral Palsy | ARSD | 414 | arylsulfatase D | P51689 |
| C0268548 | Hyperargininemia | ARSD | 414 | arylsulfatase D | P51689 |
| C0035220 | Respiratory Distress Syndrome, Newborn | ARSD | 414 | arylsulfatase D | P51689 |
| C0018798 | Congenital Heart Defects | ARSD | 414 | arylsulfatase D | P51689 |
| C1541923 | Infective endocarditis | ARSD | 414 | arylsulfatase D | P51689 |
