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CTGA Database Listing
Arab Genomic Studies
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  • Ichthyosis, Congenital, Autosomal Recessive, 10
    OMIM # 615024
    ARCI10
  • Patatin-Like Phospholipase Domain-Containing Protein 1
    OMIM # 612121
    PNPLA1
  • 3-Methylcrotonyl-CoA Carboxylase 2
    OMIM # 609014
    MCCC2, 3-Methylcrotonyl-CoA Carboxylase, Beta , MCCB, 3-Methylcrotonyl-CoA Carboxylase, Non-Biotin-Containing Subunit
  • 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency
    OMIM # 210210
    MCC2D, MCC2 Deficiency, 3-Methylcrotonylglycinuria II, Methylcrotonylglycinuria, Type II
  • Epileptic Encephalopathy, Early Infantile, 18
    OMIM # 615476
    EIEE18
  • SZT2 Subunit of KICSTOR Complex
    OMIM # 615463
    SZT2, Seizure Threshold 2, Mouse Homolog of, KIAA0467
  • Hypotonia, Infantile, with Psychomotor Retardation and Characteristic Facies 2
    OMIM # 616801
    IHPRF2
  • UNC80 Homolog, NALCN Channel Complex Subunit
    OMIM # 612636
    UNC80, UNC80, C. elegans, Homolog of, Chromosome 2 Open Reding Frame 21, C2ORF21, KIAA1843
  • Collagen, Type IV, Alpha-4
    OMIM # 120131
    COL4A4, Collagen Of Basement Membrane, Alpha-4 Chain
  • Alport Syndrome 2, Autosomal Recessive
    OMIM # 203780
    ATS2
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