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CTGA Database Listing
Arab Genomic Studies
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  • Twinkle mtDNA Helicase
    OMIM # 606075
    TWNK, Chromosome 10 Open Reading Frame 2, C10ORF2, T7 Gene 4-Like Protein with Intramitochondrial Nucleoid Localization, Twinkle, p72
  • Mitochondrial DNA Depletion Syndrome 7 (Hepatocerebral Type)
    OMIM # 271245
    MTDPS7, Spinocerebellar Ataxia, Infantile-Onset, IOSCA, Ophthalmoplegia, Hypotonia, Ataxia, Hypoacusis, and Athetosis, OHAHA Syndrome, Spinocerebellar Ataxia, Infantile. with Sensory Neuropathy, Spinocerebellar Ataxia 8, SCA8
  • Succinate Dehydrogenase Complex, Subunit A, Flavoprotein
    OMIM # 600857
    SDHA, Succinate Dehydrogenase 1, S. cerevisiae, Homolog of, SDH1, Homolog of
  • Pyruvate Dehydrogenase, Alpha-1
    OMIM # 300502
    PDHA1, Pyruvate Dehydrogenase Complex, E1-Alpha Polypeptide 1; PHE1A, PDHCE1A, PDHA
  • Pyruvate Dehydrogenase E1-Alpha Deficiency
    OMIM # 312170
    PDHAD, Pyruvate Dehydrogenase Complex Deficiency, Pyruvate Decarboxylase Deficiency, Ataxia, Intermittent, with Abnormal Pyruvate Metabolism, PDH Deficiency, Ataxia, Intermittent, with Pyruvate Dehydrogenase Deficiency, Ataxia, with Lactic Acidosis I,
  • Leigh Syndrome
    OMIM # 256000
    Necrotizing Encephalopathy, Infantile Subacute, Of Leigh, SNE, Leigh Syndrome Due To Mitochondrial Complex I Deficiency, Leigh Syndrome Due To Mitochondrial Complex II Deficiency, Leigh Syndrome Due To Mitochondrial Complex III Deficiency, Leigh Syndrome Due To Mitochondrial Complex IV Deficiency, Leigh Syndrome Due To Mitochondrial Complex V Deficiency,
  • Complex I, Subunit ND5
    OMIM # 516005
    MTND5, NADH-Ubiquinone Oxidoreductase, Subunit ND5, NADH Dehydrogenase, Subunit 5
  • Mitochondrial Myopathy, Infantile, Transient
    OMIM # 500009
    MMIT, Mitochondrial Myopathy, Infantile, Transient, due to Respiratory Chain Deficiency, COX Defieiency Myopathy, Infantile, Transient, Respiratory Chain Deficiency, Infantile Transient
  • Transfer RNA, Mitochondrial, Alanine
    OMIM # 590000
    tRNA-ALA, Mitochondrial
  • Neurexin I
    OMIM # 600565
    NRXN1
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