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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 ▲ |
|---|---|---|---|---|---|
| C0017168 | Gastroesophageal reflux disease | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0020538 | Hypertensive disease | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C4048158 | Convulsions | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0270844 | Tonic Seizures | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0751229 | Hypersomnolence | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0038220 | Status Epilepticus | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0022116 | Ischemia | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0011570 | Mental Depression | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0022333 | Jacksonian Seizure | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0236736 | Cocaine-Related Disorders | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0003469 | Anxiety Disorders | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0001973 | Alcoholic Intoxication, Chronic | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0234533 | Generalized seizures | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0023520 | Leukodystrophy | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0494475 | Tonic - clonic seizures | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0234535 | Clonic Seizures | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0740858 | Substance abuse problem | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0013336 | Dwarfism | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0235946 | Cerebral atrophy | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0282577 | Congenital Disorders of Glycosylation | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0017168 | Gastroesophageal reflux disease | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0020295 | Hydronephrosis | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0241005 | Creatine phosphokinase serum increased | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C0020615 | Hypoglycemia | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
| C2931010 | Congenital disorder of glycosylation type 2E | COG7 | 91949 | component of oligomeric golgi complex 7 | P83436 |
