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CTGA Database Listing
Arab Genomic Studies
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  • Neuropathy, Congenital Hypomyleinating, 3
    OMIM # 618186
    CHN3
  • Contactin-Associated Protein 1
    OMIM # 602346
    CNTNAP1, Contactin-Associated Protein, CASPR, Contactin-Associated Transmembrane Receptor, p190, Neurexin IV, NRXN4, Paranodin, NCP1
  • Fukutin-Related Protein
    OMIM # 606596
    FKRP
  • Muscular Dystrophy-Dystroglycanopathy (Limb-Girdle), Type C, 5
    OMIM # 607155
    MDDGC5, Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 9, LGMDR9, LGMD2I, Muscular Dystrophy, Limb-Girdle, Type 2I , Muscular Dystrophy-Dystroglyccanopathy, Limb-Girdle, FRKP-Related
  • CLN8 Gene
    OMIM # 607837
    CLN8
  • Propionyl-CoA Carboxylase, Alpha Subunit
    OMIM # 232000
    PCCA, PCCA Complementation Group
  • Ceroid Lipofuscinosis, Neuronal, 8
    OMIM # 600143
    CLN8
  • Leukoencephalopathy with Vanishing White Matter
    OMIM # 603896
    VWM, Childhood Ataxia with Central Nervous System Hypomyelinization, CACH, Vanishing White Matter Leukodystrophy, Cree Leukoencephalopathy, CLE, Vanishing White Matter Leukodystrophy with Ovarian Failure, Included, Ovarioleukodystrophy, Included,
  • Eukaryotic Translation Initiation Factor 2B, Subunit 5
    OMIM # 603945
    EIF2B5, Eukaryotic Translation Initiation Factor 2B, Epsilon, EIF2B-Epsilon
  • Phospholipase A2, Group VI
    OMIM # 603604
    PLA2G6, Phospholipase A2, Calcium-Independent, IPLA2, Patatin-Like Phospholipase Domain-Containing Protein 9, PNPLA9, Phospholipase A2, Calcium-Independent, Group VI, A, IPLA2-VIA
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