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CTGA Database Listing
Arab Genomic Studies
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  • Hennekam Lymphangiectasia-Lymphedema Syndrome
    OMIM # 235510
    Hennekam Syndrome, Lymphatic Dysplasia, Generalized,
  • Collagen and Calcium-Binding EGF Domain-Containing Protein
    OMIM # 612753
    CCBE1, KIAA1983
  • Glutaric Acidemia I
    OMIM # 231670
    Glutaric Aciduria I, GA I, Glutaryl-CoA Dehydrogenase Deficiency, GDD
  • Glutaryl-CoA Dehydrogenase
    OMIM # 608801
    GCDH
  • GM1-Gangliosidosis, Type I
    OMIM # 230500
    Gangliosidosis, Generalized GM1, Type I, Gangliosidosis, Generalized GM1, Infantile Form, Gangliosidosis, Generalized GM1, Type 1, Beta-Galactosidase-1 Deficiency, GLB1 Deficiency, GM1-Gangliosidosis, Type I, With Cardiac Involvement, Gangliosidosis, Generalized GM1, Type I, With Cardiac Involvement
  • Galactosidase, Beta-1
    OMIM # 611458
    GLB1, Beta-Galactosidase-1, Elastin-Binding Protein, EBP, S-GAL, Elastin Recepror 1,
  • Farber Lipogranulomatosis
    OMIM # 228000
    FRBRL, Farber Disease, Ceramidase Deficiency, Acid Ceramidase Deficiency, AC Deficiency, N-Laurylsphingosine Deacylase Deficiency
  • N-Acylsphingosine Amidohydrolase 1
    OMIM # 613468
    ASAH1, ASAH, N-Acylsphingosine Deacylase, Acid Ceramidase, AC, Acid CDase, ACDase
  • Aarskog-Scott Syndrome
    OMIM # 305400
    AAS, Faciogenital Dysplasia, FGDY, Faciodigitogenital Syndrome, Aarskog Syndrome, X-Linked, Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder, Mental Retardation, X-Linked, Syndromic 16, MRXS16,
  • FYVE, RhoGEF, and PH Domain-Containing Protein 1
    OMIM # 300546
    FGD1
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