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CTGA Database Listing
Arab Genomic Studies
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  • Amelogenesis Imperfecta, Hypomaturation Type, IIA3
    OMIM # 613211
    AI2A3
  • Weill-Marchesani-like Syndrome
    OMIM # 613195
  • Purine Nucleoside Phosphorylase Deficiency
    OMIM # 613179
    Nucleoside Phosphorylase Deficiency
  • Neuropathy, Hereditary Sensory and Autonomic, Type IIB
    OMIM # 613115
    HSAN2B
  • Polycystic Kidney Disease 2
    OMIM # 613095
    PKD2, Polucystic Kidney Disease, Adult, Type II, APKD2
  • Leukemia, Acute Lymphoblastic
    OMIM # 613065
    ALL, Leukemia, Acute Lymphoblastic, Susceptibility to, 1, ALL1, Leukemia, Acute Lymphocytic, Susceptibility to, 1, Leukemia, B-Cell Acute Lymphoblastic, Susceptibility to, Leukemia, T-Cell Acute Lymphoblastic, Susceptibility to, Leukemia, Acute Lymphoblastic, B-Hyperdiploid, Susceptibility to
  • Pituitary Hormone Deficiency, Combined, 1
    OMIM # 613038
    CPHD1
  • Cutis Laxa, Autosomal Recessive, Type IIB
    OMIM # 612940
    ARCL2B, Cutis Laxa with Progeroid Features,
  • LFNG O-Fucosylpeptide 3-Beta-N-Acetylglucosaminyltransferase
    OMIM # 602576
    LFNG
  • Spondylocostal Dysostosis 3, Autosomal Recessive
    OMIM # 609813
    SCDO3,
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