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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 |
|---|---|---|---|---|---|
| C0017601 | Glaucoma | ARSD | 414 | arylsulfatase D | P51689 |
| C0018802 | Congestive heart failure | ARSD | 414 | arylsulfatase D | P51689 |
| C0678222 | Breast Carcinoma | ARSD | 414 | arylsulfatase D | P51689 |
| C0020538 | Hypertensive disease | ARSD | 414 | arylsulfatase D | P51689 |
| C0268547 | Argininosuccinic Aciduria | ARSD | 414 | arylsulfatase D | P51689 |
| C0037789 | Specific reading disorder | ARSD | 414 | arylsulfatase D | P51689 |
| C0009460 | Communication impairment | ARSD | 414 | arylsulfatase D | P51689 |
| C0476254 | Dyslexia | ARSD | 414 | arylsulfatase D | P51689 |
| C0003076 | Aniridia | ARSD | 414 | arylsulfatase D | P51689 |
| C0004364 | Autoimmune Diseases | ARSD | 414 | arylsulfatase D | P51689 |
| C0007222 | Cardiovascular Diseases | ARSD | 414 | arylsulfatase D | P51689 |
| C0878544 | Cardiomyopathies | ARSD | 414 | arylsulfatase D | P51689 |
| C0175695 | Sotos' syndrome | ARSD | 414 | arylsulfatase D | P51689 |
| C0023186 | Learning Disorders | ARSD | 414 | arylsulfatase D | P51689 |
| C0004930 | Behavior Disorders | ARSD | 414 | arylsulfatase D | P51689 |
| C0011757 | Developmental Coordination Disorder | ARSD | 414 | arylsulfatase D | P51689 |
| C0036857 | Severe intellectual disability | ARSD | 414 | arylsulfatase D | P51689 |
| C0022672 | Acute Kidney Tubular Necrosis | ARSD | 414 | arylsulfatase D | P51689 |
| C0086132 | Depressive Symptoms | ARSD | 414 | arylsulfatase D | P51689 |
| C0339573 | Glaucoma, Primary Open Angle | ARSD | 414 | arylsulfatase D | P51689 |
| C0028043 | Nicotine Dependence | ARSD | 414 | arylsulfatase D | P51689 |
| C0003507 | Aortic Valve Stenosis | ARSD | 414 | arylsulfatase D | P51689 |
| C0013080 | Down Syndrome | ARSD | 414 | arylsulfatase D | P51689 |
| C0020302 | Hydrophthalmos | ARSD | 414 | arylsulfatase D | P51689 |
| C0032897 | Prader-Willi Syndrome | ARSD | 414 | arylsulfatase D | P51689 |
