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CTGA Database Listing
Arab Genomic Studies
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  • Spinocerebellar Ataxia, Autosomal Recessive 12
    OMIM # 614322
    SCAR12, Spinocerebellar Ataxia with Mental Retardation and Epilepsy,
  • SWI/SNF-Related, Matrix-Associated, Actin-Dependent Regulator of Chromatin, Subfamily A-Like Protein 1
    OMIM # 606622
    SMARCAL1, SMARCA-Like Protein 1, HepA-Related Protein, HARP
  • Kleine-Levin Hibernation Syndrome
    OMIM # 148840
    Kleine-Levin Syndrome
  • Ichthyosis, Lamellar, Autosomal Dominant
    OMIM # 146750
    Lamellar Ichthyosis, Autosomal Dominant
  • Ubiquitin-Protein Ligase E3 Component N-Recognin 1
    OMIM # 605981
    UBR1, Ubiquitin Protein Ligase E3 Component N-Recognin , Ubiquitin-Protein Ligase E3-Alpha-1, Ubiquitin-Protein Ligase E3-Alpha-I, N-Recognin-1, Ubiquitin-Protein Ligase E3-Alpha 3, Ubiquitin Ligase E3 Alpha-I, E3a Ligase , EC, JBS,
  • Arthrogryposis, Perthes Disease, and Upward Gaze Palsy
    OMIM # 614262
    APUG
  • Charcot-Marie-Tooth Disease, Type 4B3
    OMIM # 615284
    CMT4B3, Charcot-Marie-Tooth disease with focally folded myelin
  • DNA Methyltransferase 3B
    OMIM # 602900
    DNMT3B, DNA (Cytosine-5-)-Methyltransferase 3 Beta, DNA Methyltransferase HsaIIIB, DNA MTase HsaIIIB, M.HsaIIIB
  • Exfoliation Syndrome
    OMIM # 177650
    XFS, Exfoliation Glaucoma, XFG, Pseudoexfoliation Glaucoma, PEXG, Pseudoexfoliation of the Lens, Pseudoexfoliation Syndrome, PEXS
  • Foveal Hypoplasia 1
    OMIM # 136520
    FVH1, Foveal Hypoplasia 1 with or without Anterior Segment Anomalies and/or Cataract, Foveal Hypoplasia-Presenile Cataract Syndrome, O'Donnell-Pappas Syndrome
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