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CTGA Database Listing
Arab Genomic Studies
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  • Aspartate Beta-Hydroxylase
    OMIM # 600582
    ASPH, Aspartyl/Asparaginyl-Beta-Hydroxylase, HAAH, BAH,
  • ZIC Family, Member 3
    OMIM # 300265
    ZIC3, Zinc Finger Protein of Cerebellum 3, HTX1,
  • Heterotaxy, Visceral, 1, X-Linked
    OMIM # 306955
    HTX1, Dextrocardia with Other Cardiac Malformations, Laterality, X-Linked, Situs Inversus, Complex Cardiac Defects, and Splenic Defects, X-Linked, Congenital Heart Defects, Multiple Types, 1, X-Linked, CHTD1
  • Alport Syndrome, X-Linked
    OMIM # 301050
    ATS, Nephropathy and Deafness, Alport Syndrome-Like Hereditary Nephritis, ASLHN, ASLN
  • Collagen, Type IV, Alpha-5
    OMIM # 303630
    COL4A5, Collagen of Basement Membrane, Alpha-5 Chain,
  • Anus, Imperforate
    OMIM # 301800
  • AU-Specific RNA-Binding Protein
    OMIM # 600529
    AUH, 3-Methylglutaconyl-CoA Hydratase
  • 3-Methylglutaconic Aciduria, Type I
    OMIM # 250950
    MGA, Type I, MGA1, 3-@Methylglutaconyl-CoA Hydratase Deficiency, 3-MG-CoA-Hydratase Deficiency
  • Autoimmune Polyendocrine Syndrome, Type I, with or without Reversible Metaphyseal Dysplasia
    OMIM # 240300
    APS1APS I, Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy, APECED, Autoimmune Polyglandular Syndrome, Type I, Polyglandular Autoimmine Syndrome, Type I, PGA I, Hypoadrenocorticism with Hypoparathyroidism and Superficial Moniliasis, Autoimmune Polyendocrinopathy Syndrome, Type I, Autosomal Dominant, Polyglandular Deficiency Syndrome, Persian-Jewish TypeYPE
  • Autoimmune Regulator
    OMIM # 607358
    AIRE
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