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CTGA Database Listing
Arab Genomic Studies
Records found: 2749 Sort by:
  • TSC2 Gene
    OMIM # 191092
    TSC2, Tuberin, TSC4 Gene, TSC4
  • Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes
    OMIM # 540000
    MELAS, MELAS Syndrome,
  • Sodium Channel, Neuronal Type I, Alpha Subunit
    OMIM # 182389
    SCN1A, Sodium Channel, Brain Type I, Alpha Subunit, NAC1, NAV1.1
  • Epileptic Encephalopathy, Early Infantile, 6
    OMIM # 607208
    EIEE6, Dravet Syndrome, Severe Myoclonic Epilepsy of Infancy, SMEI
  • Laminin, Alpha-2
    OMIM # 156225
    LAMA2, Laminin 2, Heavy Chain, Merosin, Laminin 2, Laminin M , LAMM,
  • Cystic Fibrosis
    OMIM # 219700
    CF, Mucoviscidosis,
  • BBS10 Gene
    OMIM # 610148
    BBS10, Chromosome 12 Open Reading Frame 58, C12ORF58, FLJ23560
  • Bardet-Biedl Syndrome 10
    OMIM # 615987
    BBS10
  • Mitochondrial Complex IV Deficiency
    OMIM # 220110
    Cytochrome c Oxidase Deficiency, COX Deficiency
  • PET100 Cytochrome c Oxidase Chaperone
    OMIM # 614770
    PET100, PET100, S. Cerevisiae, Homolog of , Chromosome 19 Open Reading Frame 79 C19ORF79
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