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CTGA Database Listing
Arab Genomic Studies
Records found: 2791 Sort by:
  • Phosphodiesterase 6B, cGMP-Specific, Rod, Beta
    OMIM # 180072
    PDE6B
  • Retinitis Pigmentosa 40
    OMIM # 613801
    RP40
  • RP1 Gene
    OMIM # 603937
    RP1, Oxygen-Regulated Photoreceptor Protein 1, ORP1,
  • Retinol Dehydrogenase 12
    OMIM # 608830
    RDH12, Retinol Dehydrogenase, All-Trans and 9-Cis,
  • Bone Mineral Density Quantitative Trait Locus 1
    OMIM # 601884
    BMND1, High bone Mass, HBM, Osteoporosis, Susceptibility
  • Coronary Artery Disease, Autosomal Dominant, 1
    OMIM # 608320
    ADCAD1
  • Arthrogryposis, Distal, Type 2A
    OMIM # 193700
    DA2A, Freeman-Sheldon Syndrome, FSS, Whistling Face-Windmill Vane Hand Syndrome, Craniocarpotarsal Dystrophy, Craniocarpotarsal Dysplasia
  • Phosphatase and Actin Regulator 1
    OMIM # 608723
    PHACTR1, KIAA1733
  • 3-Methylcrotonyl-CoA Carboxylase 1
    OMIM # 609010
    MCCC1, 3-Methylcrotonyl-CoA Carboxylase, Alpha, MCCA, 3-Methylcrotonyl-CoA Carboxylase, Biotin-Containing Subunit
  • 3-Methylcrotonyl-CoA Carboxylase 1 Deficiency
    OMIM # 210200
    MCC1D, MCCD Type 1, MCC1 Deficiency, 3-Methylcrotonylglycinuria I, Methylcrotonylglycinuria Type I
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