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CTGA Database Listing
Arab Genomic Studies
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  • A Disintegrin and Metalloproteinase Domain 17
    OMIM # 603639
    ADAM17, Tumor Necrosis Factor-Alpha Converting Enzyme, TACE
  • Immunodeficiency, Common Variable, 8, with Autoimmunity
    OMIM # 614700
    CVID8
  • Lipopolysaccharide-Responsive, Beige-Like Anchor Protein
    OMIM # 606453
    LRBA, LBA, Cell Division Cycle 4-Like Protein, CDC4L, Cdc4-Like Protein,
  • Inflammatory Bowel Disease 28, Autosomal Recessive
    OMIM # 613148
    IBD28, Inflammatory Bowel Disease, Early-Onset, Autosomal Recessive,
  • Interleukin 10 Receptor, Alpha
    OMIM # 146933
    IL10RA, Interleukin 10 Receptor, IL10R, IL10R1,
  • Immunodeficiency 56
    OMIM # 615207
    IMD56, IL21R Immunodeficiency,
  • Interleukin 21 Receptor
    OMIM # 605383
    IL21R, IL21R/BCL6 Fusion Gene,
  • Atrial Septal Defect 7 with or without Atrioventricular Conduction Defects
    OMIM # 108900
    ASD7 , ASD with or without Atrioventricular Conduction Defects
  • NK2 Homeobox 5
    OMIM # 600584
    NKX2-5 , NK2, Drosophila, Homolog of, E , NKX2E, Cardiac-Specific Homeobox 1, CSX1, CSX, NKX2.5, Mouse, Homolog of
  • Spinocerebellar Ataxia, Autosomal Recessive 2
    OMIM # 213200
    SCAR2, Cerebelloparenchymal Disorder III, CPD III, CPD3, Cerebellar Hypoplasia, Nonprogressive Norman Type, Cerebellar Granular Cell Hypoplasia and Mental Retardation, Congenital
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