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CTGA Database Listing
Arab Genomic Studies
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  • Coagulation Factor V
    OMIM # 612309
    F5, Protein C Cofactor, PCCF, Activated Protein C Cofactor, APC Cofactor, Labile Factor, Factor V Leiden
  • Thrombophilia due to Activated Protein C Resistance
    OMIM # 188055
    THPH2, Activated Protein C Resistance, APC Resistance, Thrombophilia due to Deficiency of Activated Protein C Cofactor, PROC Cofactor Deficiency, PCCF Deficiency, Thrombophilia V, Thrombophilia due to Factor V Leiden
  • Leber Congenital Amaurosis 6
    OMIM # 613826
    LCA6
  • Peroxisome Biogenesis Factor 6
    OMIM # 601498
    PEX6, Peroxin 6, Peroxisomal Assembly Factor 2, PAF2, Peroxisomal-Type ATPase 1, PXAAA1,
  • Peroxisome Biogenesis Disorder 4A (Zellweger)
    OMIM # 614862
    PBD4A, Peroxisome Biogenesis Disorder, Complementation Group 4, CG4, Peroxisome Biogenesis Disorder, Complementation Group 6, CG6, Peroxisome Biogenesis Disorder, Complementation Group C, CGC
  • Peroxisome Biogenesis Factor 16
    OMIM # 603360
    PEX16, Peroxin 16
  • Peroxisome Biogenesis Disorder 8B
    OMIM # 614877
    PBD8B
  • Hydrocephalus, Nonsyndromic, Autosomal Recessive 2
    OMIM # 615219
    HYC2
  • Multiple PDZ Domain Protein
    OMIM # 603785
    MPDZ, MUPP1
  • Cone-Rod Dystrophy 13
    OMIM # 608194
    CORD13
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