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CTGA Database Listing
Arab Genomic Studies
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  • Nemaline Myopathy 3
    OMIM # 161800
    NEM3, Myopathy, Actin, Congenital, with Excess of Thin Myofilaments, Included, Nemaline Myopathy 3, with Intranuclear Rods, Included, Myopathy, Actin, Congenital, with Cores, Included,
  • Actin, Alpha, Skeletal Muscle 1
    OMIM # 102610
    ACTA1, ASMA,
  • Myocardial Infarction, Susceptibility to, 1
    OMIM # 608446
    MCI1, Myocardial Infarction, Early-Onset, Susceptibility to,
  • ALMS1 Gene
    OMIM # 606844
    ALMS1, KIAA0328,
  • Guanylate Cyclase 2D, Membrane
    OMIM # 600179
    GUCY2D, GUC2D, Guanylate Cyclase 2D, Retinal, GUCY2E, Mouse, Homolog of, Rod Outer Segment Membrane Guanylate Cyclase, ROSGC, RETGC, RETGC1
  • Rheumatic Fever-Related Antigen
    OMIM # 268240
    Rheumatic Fever, Acute, Susceptibility to
  • Ichthyosis, Lamellar, 1
    OMIM # 242300
    LI1, Ichthyosis Congenita, Lamellar Exfoliation of Newborn, Desquamation of Newborn, Collodion Fetus, Lamellar Ichthyosis, LI, Lamellar Ichthyosis, Type 1, Ichthyosis Congenita II, ICR2, Self-Healing Collodion Baby,
  • Leber Congenital Amaurosis 1
    OMIM # 204000
    LCA1, Amaurosis Congenita of Leber I, LCA, Retinal Blindness, Congenital , CRB
  • Alstrom Syndrome
    OMIM # 203800
    ALMS, ALSS
  • Transglutaminase 1
    OMIM # 190195
    TGM1, Transglutaminase, Keratinocyte, TGK, Transglutaminase, Epidermal Type I,
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