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CTGA Database Listing
Arab Genomic Studies
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  • SZT2 Subunit of KICSTOR Complex
    OMIM # 615463
    SZT2, Seizure Threshold 2, Mouse Homolog of, KIAA0467
  • Hypotonia, Infantile, with Psychomotor Retardation and Characteristic Facies 2
    OMIM # 616801
    IHPRF2
  • UNC80 Homolog, NALCN Channel Complex Subunit
    OMIM # 612636
    UNC80, UNC80, C. elegans, Homolog of, Chromosome 2 Open Reding Frame 21, C2ORF21, KIAA1843
  • Collagen, Type IV, Alpha-4
    OMIM # 120131
    COL4A4, Collagen Of Basement Membrane, Alpha-4 Chain
  • Alport Syndrome 2, Autosomal Recessive
    OMIM # 203780
    ATS2
  • Muscular Dystrophy, Congenital Merosin-Deficient, 1A
    OMIM # 607855
    MDC1A, Muscular Dystrophy, Congenital Merosin-Deficient, Muscular Dystrophy, Congenital, Due to Partial LAMA2 Deficiency
  • Leukemia, Acute Myeloid
    OMIM # 601626
    AML, Leukemia, Acute Myelogenous, Acute Myeloblastic Leukemia, Acute Granulocytic Leukemia, Acute Nonlymphocytic Leukemia
  • Ataxia-Telangiectasia Mutated Gene
    OMIM # 607585
    ATM
  • Ataxia-Telangiectasia
    OMIM # 208900
    AT, AT1, Louis-Bar Syndrome, AT, Complementation Group A, ATA, AT, Complementation Group C, ATC, AT, Complementation Group D, ATD, AT, Complementation Group E, ATE, Ataxia-Telangiectasia Variant
  • Netherton Syndrome
    OMIM # 256500
    NETH, NS, Netherton Disease, Bamboo Hair Syndrome, Trichorrhexis Invaginata,
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