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CTGA Database Listing
Arab Genomic Studies
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  • Wilson Disease
    OMIM # 277900
    WND, WD, Hepatolenticular Degeneration
  • A Disintegrin-Like and Metalloproteinase with Thrombospondin Type 1 Motif, 10
    OMIM # 608990
    ADAMTS10
  • Weill-Marchesani Syndrome, Autosomal Recessive
    OMIM # 277600
    WM Syndrome, WMS, Spherophakia-Brachymorphia Syndrome, Mesodermal Dysmorphodystrophy, Congenital,
  • Cytotoxic T Lymphocyte-Associated 4
    OMIM # 123890
    CTLA4, CD152, Cytotoxic T Lymphocyte-Associated 4, Soluble Isoform
  • Graves Disease
    OMIM # 275000
    GRD, Thyrotoxicosis, Hyperthyroidism, Autoimmune, GRD1, Graves Disease, Susceptibility to, 1,
  • Tetra-Amelia, Autosomal Recessive
    OMIM # 273395
    TETAMS, Autosomal Recessive Tetra-Amelia, Autosomal Recessive Tetraamelia,
  • Hexosaminidase A
    OMIM # 606869
    Beta-Hexosaminidase A, HEXA
  • Tay-Sachs Disease
    OMIM # 272800
    TSD, Gangliosidosis, Type I, B Variant GM2-Gangliosidosis, Hexosaminidase A Deficiency, HEXA Deficiency, Tay-Sachs Disease, Juvenile, Hexosaminidase A Deficiency, Adult Type, GM2-Gangliosidosis, Adult Chronic Type, Tay-Sachs Disease, Variant B1, Tay-Sachs Disease, Pseudo-AB Variant
  • Lipodystrophy, Congenital Generalized, Type 2
    OMIM # 269700
    CGL2, Berardinelli-Seip Congenital Lipodystrophy Type 2, Seip Syndrome, Berardinelli Syndrome, Lipodystrophy, Total, and Acromegaloid Gigantism, Congenital Lipoatrophic Diabetes, Lipodystrophy, Berardinelli-Seip Congenital Type 2, Brunzell Syndrome, Brunzell Syndrome, BSCL2-Related
  • BSCL2 Gene
    OMIM # 606158
    BSCL2 , Seipin, GNG3LG, Mouse, Homolog of,
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