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 59276 - 59300 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0011269 Dementia, Vascular SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0022336 Creutzfeldt-Jakob disease SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0011570 Mental Depression SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0494463 Alzheimer Disease, Late Onset SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0004153 Atherosclerosis SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0338451 Frontotemporal dementia SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0242383 Age related macular degeneration SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0036572 Seizures SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C3501372 Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0011847 Diabetes SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0344315 Depressed mood SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C3665347 Visual Impairment SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0023530 Leukopenia SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0029089 Ophthalmoplegia SUCLA2 8803 succinate-CoA ligase ADP-forming subunit beta Q9P2R7
C0023264 Leigh Disease SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C2931891 Necrotizing encephalopathy, infantile subacute, of Leigh SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C1850598 Leigh Syndrome due to Mitochondrial Complex III Deficiency SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C1838951 LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C0342782 Depletion of mitochondrial DNA SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C1850600 Leigh Syndrome due to Mitochondrial Complex V Deficiency SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C1850597 Leigh Syndrome Due To Mitochondrial Complex II Deficiency SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C3151476 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITH METHYLMALONIC ACIDURIA) SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C0036572 Seizures SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C0007194 Hypertrophic Cardiomyopathy SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597
C3711369 Succinate-Coa Ligase Deficiency SUCLG1 8802 succinate-CoA ligase GDP/ADP-forming subunit alpha P53597

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