3645
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Succinate-CoA ligase ADP-forming subunit beta |
A-BETA, A-SCS, LINC00444, MTDPS5, SCS-betaA |
Curated: Color vision deficiency, Colorectal cancer, Mitochondrial dna depletion syndrome, Peritoneal disease, Eosinophilia, Global developmental delay, Leigh syndrome, Obesity, Oligodendroglioma, mitochondrial disease
Unreviewed: Agammaglobulinemia, Age-related macular degeneration, Alzheimer disease, Amnesia, Amyloidosis, Anemia, Arteriosclerosis, Atherosclerosis, Aural Atresia, Congenital, Brain disease, Breast neoplasm, Cerebral amyloid angiopathy, Cerebral Atrophy, Chorea, Choreoathetosis, Coenzyme q10 deficiency, Cognitive disorder, Congestive Heart Failure, Crohn Disease, Deafness, Dementia, Developmental Delay, Diabetes, Diabetes Mellitus, Down Syndrome, Dwarfism, Dystonia, Epilepsy, Erythropoietic Protoporphyria, Frontotemporal dementia, Hearing Loss, Heart Failure, Hepatocellular carcinoma, Hypercholesterolemia, Impaired Cognition, Lactic acidosis, Leigh Syndrome, Leukopenia, Lewy Body Disease, Mental Depression, Methylmalonic acidemia, Microcephaly, Mitochondrial disease, Mitochondrial encephalomyopathy, Movement disorder, Movement Disorders, Multiple myeloma, Myelodysplastic syndrome, Myoclonic dystonia, Necrotizing encephalomyelopathy, Nervous System Diseases, Nervous System Disorder, Neuroblastoma, Neurodegenerative Disorders, Parkinson disease, Polyneuropathy, Ptosis, Renal cell carcinoma, Retinoblastoma, Senile Dementia, Senile Plaques, Sideroblastic Anemia, X-Linked, Strabismus, Trichohepatoenteric Syndrome, Visceral neuropathy
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3650
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Succinate-CoA ligase GDP/ADP-forming subunit alpha |
GALPHA, MTDPS9, SUCLA1 |
Curated: Astrocytoma, Mitochondrial dna depletion syndrome, Leigh syndrome, Stomach neoplasms
Unreviewed: Alzheimer disease, Aphasia, Cerebral Atrophy, Developmental Delay, Developmental disability, Epileptic encephalopathy, Gastric Cancer, Glioblastoma, Glioma, Hepatocellular carcinoma, Hypertrophic cardiomyopathy, Hypoglycemia, Lactic acidosis, Leigh Syndrome, McCune-Albright Syndrome, Mental retardation, Methylmalonic acidemia, Mitochondrial disease, Mitochondrial DNA Depletion Syndrome, Mitochondrial encephalomyopathy, Necrotizing encephalomyelopathy, Night blindness, congenital stationary, Ovarian diseases, Ovarian hyperstimulation syndrome, Parkinson disease, Respiratory Failure, Stomach Neoplasms, Uveal melanoma, Visceral neuropathy
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