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CTGA Database Listing
Arab Genomic Studies
Records found: 2810 Sort by:
  • Mitochondrial DNA Depletion Syndrome 4A (Alpers Type)
    OMIM # 203700
    MTDPS4A, Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis, Alpers Progressive Infantile Poliodystrophy, Alpers Syndrome, Alpers-Huttenlocher Syndrome, Neuronal Degeneration of Childhood with Liver Disease, Progressive, PNDC
  • Polymerase, DNA, Gamma
    OMIM # 174763
    POLG, Polymerase, DNA, Gamma-1, POLG1, POLG, Catalytic Subunit, POLG-Alpha, POLGA
  • Thrombophilia due to thrombin defect
    OMIM # 188050
    THPH1, Thrombophilia due to Factor 2 Defect, Venous Thrombosis, Venous Thromboembolism, VTE, Thrombosis, protection Against,
  • Coronary Heart Disease, Susceptibility to, 1
    OMIM # 607339
    CHDS1
  • Acyl-CoA Dehydrogenase, Medium-Chain, Deficiency of
    OMIM # 201450
    ACADMD, ACADM Deficiency, MCAD Deficiency, MCADH Deficiency, Carnitine Deficiency Secondary to Medium-Chain Acyl-CoA, Dehydrogenase Deficiency
  • Acyl-CoA Dehydrogenase, Medium-Chain
    OMIM # 607008
    ACADM, Medium-Chain Acyl-CoA Dehydrogenase, MCAD, MCADH,
  • Pregnancy Loss, Recurrent, Susceptibility to, 2
    OMIM # 614390
    RPRGL2
  • Pregnancy Loss, Recurrent, Susceptibility to, 1
    OMIM # 614389
    RPRGL1, RPRGL, RPL, Abortion, Spontaneous, Recurrent, Fetal Loss, Recurrent, Susceptibility to, Miscarriage, Recurrent, Embryonic Loss, Recurrent, Stillbirth, Recurrent
  • Retinitis Pigmentosa 56
    OMIM # 613581
    RP56
  • Interphotoreceptor Matrix Proteoglycan 2
    OMIM # 607056
    IMPG2, SPACRCAN, IPM200
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