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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • Pejvakin
    OMIM # 610219
    PJVK, DFNB59 Gene
  • Deafness, Autosomal Recessive 59
    OMIM # 610220
    DFNB59
  • Retinitis Pigmentosa 38
    OMIM # 613862
    RP38, Rod-Cone Dystrophy, Childhood-Onset
  • MER Tyrosine Kinase Protooncogene
    OMIM # 604705
    MERTK
  • Very Low Density Lipoprotein Receptor
    OMIM # 192977
    VLDLR
  • Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1
    OMIM # 224050
    CAMRQ1, Cerebellar Hypoplasia, VLDLR-Associated, Cerebellar Ataxia and Mental Retardation with or without Quadrupedal Locomotion 1, Cerebellar Ataxia, Congenital, and Mental Retardation, Autosomal Recessive, Dysequilibrium Syndrome, DES
  • F-Box Only Protein 32
    OMIM # 606604
    FBXO32, Muscle Atrophy F-Box, MAFBX, Atrophy Gene 1, ATROGIN1, FLJ32424,
  • Chondrodysplasia, Grebe Type
    OMIM # 200700
    Achondrogenesis, Brazilian, Grebe Chondrodysplasia, Grebe Dysplasia, Acromesomelic Dysplasia, Grebe Type, AMDG, Achondrogenesis, Type II, Formerly,
  • Growth/Differentiation Factor 5
    OMIM # 601146
    GDF5, Cartilage-Derived Morphogenetic Protein 1, CDMP1, Lipopolysaccharide-Associated Protein 4, LAP4, LPS-Associated Protein 4, Bone Morphogenetic Protein 14, BMP14,
  • Retinitis Pigmentosa 80
    OMIM # 617781
    RP80
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