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CTGA Database Listing
Arab Genomic Studies
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  • Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 2
    OMIM # 601460
    PHOAR2 , Pachydermoperiostosis, Autosomal Recessive , PDP, Autosomal Recessive,
  • Solute Carrier Organic Anion Transporter Family, Member 2A1
    OMIM # 614441
    SLCO2A1 , Organic Anion Transporter 2A1 , OATP2A1, Prostaglandin Transporter , PGT, Solute Carrier Family 21 (Prostaglandin Transporter), Member 2, Formerly , SLC21A2, Formerly
  • T-Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
    OMIM # 601705
  • Forkhead Box N1
    OMIM # 600838
    FOXN1 , Winged Helix Nude , WHN
  • Cutis Laxa, Autosomal Recessive, Type IA
    OMIM # 219100
    ARCL1A, ARCL1, Cutis Laxa, Autosomal Recessive
  • Fibulin 5
    OMIM # 604580
    FBLN5 , Developmental Arteries and Neural Crest EGF-Like, DANCE
  • Hypotrichosis 7
    OMIM # 604379
    HYPT7, Hypotrichosis, Localized, Autosomal Recessive 2 , LAH2, Hypotrichosis, Autosomal Recessive , AH, Hypotrichosis, Total, Mari Type , Woolly Hair, Autosomal Recessive 2, with or without Hypotrichosis , ARWH2, WH/HT
  • Lipase H
    OMIM # 607365
    LIPH, Membrane Associated Phoshatidic Acid-Selective Phospholipase A1 , MPAPLA1, Phospholipase A1, Phosphatidic Acid-Selective, Membrane-Associated , LPD Lipase-Related Protein, LPDLR
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
    OMIM # 610476
    ARVD11 , Arrhythmogenic Right Ventricular Cardiomyopathy 11 , ARVC11 , Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 with Mild Palmoplantar Keratoderma with or without Woolly Hair
  • Desmocollin-2
    OMIM # 125645
    Desmocollin 3, Formerly, DSC3, Formerly, Desmosomal Glycoprotein II/III, DG2/3, DG2
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