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
Displaying entries 62201 - 62225 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0029408 Degenerative polyarthritis ABAT 18 4-aminobutyrate aminotransferase P80404
C0002622 Amnesia ABAT 18 4-aminobutyrate aminotransferase P80404
C0019337 Heroin Dependence ABAT 18 4-aminobutyrate aminotransferase P80404
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
C0302362 Brucella melitensis infection OXSM 54995 3-oxoacyl-ACP synthase, mitochondrial Q9NWU1
C0041296 Tuberculosis OXSM 54995 3-oxoacyl-ACP synthase, mitochondrial Q9NWU1
C0006142 Malignant neoplasm of breast OXSM 54995 3-oxoacyl-ACP synthase, mitochondrial Q9NWU1
C0029459 Osteoporosis, Senile OXCT1 5019 3-oxoacid CoA-transferase 1 P55809
C1536500 Deficiency of acetyl-CoA acetyltransferase OXCT1 5019 3-oxoacid CoA-transferase 1 P55809

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Last updated: August 19, 2024