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CTGA Database Listing
Arab Genomic Studies
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  • Wolframin ER Transmembrane Glycoprotein
    OMIM # 606201
    WFS1, Wolframin
  • Wolfram Syndrome 1
    OMIM # 222300
    WFS1, WFS, Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness, DIDMOAD
  • RAB3 GTPase-Activating Protein, Catalytic Subunit
    OMIM # 602536
    RAB3GAP1, RAB3GAP, RAB3GAP, 130-KD Subunit, RAB3GAP, Catalytic Subunit, p130, WARBM1 Gene, KIAA0066
  • Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2
    OMIM # 607473
    VKCFD2
  • Coumarin Resistance
    OMIM # 122700
    Coumarin, Poor metabolism of, Warfarin Resistance, Coumarin Sensitivity, Warfarin Sensitivity,
  • Kearns-Sayre Syndrome
    OMIM # 530000
    KSS, Chronic Progressive External Ophthalmoplegia, CPEO, Ophthalmoplegia, Pigmentary Degeneration of Retina, and Cardiomyopathy, Oculocraniosomatic Syndrome, Ophthalmoplegia-Plus Syndrome, Mitochondrial Cytopathy, Ophthalmoplegia, Progressive External, with Ragged-Red Fibers, Chronic Progressive External Ophthalmoplegia with Myopathy, CPEO with Myopathy, CPEO with Ragged-Red Fibers
  • Usher Syndrome, Type IC
    OMIM # 276904
    USH1C, Usher Syndrome, Type I, Acadian Variety
  • Transposition of the Great Arteries, Dextro-Looped
    OMIM # 608808
    DTGA, D-TGA
  • Transcobalamin II Deficiency
    OMIM # 275350
    TC II Deficiency, TCN2 Deficiency
  • Transcobalamin II
    OMIM # 613441
    TCN2, TC II, Vitamin B-12 Binding Protein 2
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