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CTGA Database Listing
Arab Genomic Studies
Records found: 2156 Sort by:
  • Retinitis Pigmentosa 55
    OMIM # 613575
    RP55
  • Retinol Dehydrogenase 12
    OMIM # 608830
    RDH12, Retinol Dehydrogenase, All-Trans and 9-Cis,
  • Microphthalmia, Isolated 6
    OMIM # 613517
    MCOP6, Microphthalmia, Posterior Nonsyndromic,
  • Mouse Double Minute 2 Homolog
    OMIM # 164785
    MDM2, p53-Binding Protein MDM2, Oncoprotein MDM2, HDM2,
  • X-Ray Repair, Complementing Defective, in Chinese Hamster, 5
    OMIM # 194364
    XRCC5, Ku Antigen, 80-kD Subunit, Ku80, Ku86,
  • Metachromatic Leukodystrophy due to Saposin B Deficiency
    OMIM # 249900
    Metachromatic Leukodystrophy due to Cerebroside Sulfatase Activator Deficiency, Saposin B Deficiency,
  • Polymerase, DNA, Epsilon-2
    OMIM # 602670
    POLE2, DPE2,
  • Weill-Marchesani-like Syndrome
    OMIM # 613195
  • Coiled-Coil and C2 Domains-Containing Protein 2A
    OMIM # 612013
    CC2D2A, KIAA1345,
  • Purine Nucleoside Phosphorylase Deficiency
    OMIM # 613179
    Nucleoside Phosphorylase Deficiency
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