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CTGA Database Listing
Arab Genomic Studies
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  • Sjogren Syndrome
    OMIM # 270150
    Sicca Syndrome
  • Schneckenbecken Dysplasia
    OMIM # 269250
    Chondrodysplasia, Lethal Neonatal, with Snail-Like Pelvis
  • Hypothyroidism, Congenital, Nongoitrous, 1
    OMIM # 275200
    CHNG1, Thyrotropin Resistance, Thyroid-Stimulating Hormone, Resistance to, RTSH, TSH Resistance, Hypothyroidism, Nonautoimmune, Hypothyroidism, Congenital, Due to TSH Resistance, Hypothyroidism Due to Unresponsiveness to Thyrotropin,
  • Mismatch Repair Cancer Syndrome
    OMIM # 276300
    MMRCS, Mismatch Repair Deficiency, MMR Deficiency, Childhood Cancer Syndrome, Brain Tumor-Polyposis Syndrome 1, BTPS1, BTP1 Syndrome, Turcot Syndrome
  • Discoidin Domain Receptor Family, Member 2
    OMIM # 191311
    DDR2, Neurotrophic Tyrosine Kinase Receptor-Related 3, NTRKR3, Tyrosine Kinase Receptor Related to Neurotrophic TRK, TKT
  • Dihydrolipoamide Dehydrogenase Deficiency
    OMIM # 246900
    DLDD, DLD Deficiency, E3 Deficiency, Lipoamide Dehydrogenase Deficiency, Lactic Acidosis due to, Maple Syrup Urine Disease, Type III,
  • Dihydrolipoamide Dehydrogenase
    OMIM # 238331
    DLD, Pyruvate Dehydrogenase Component E3, PHE3, E3, Branched Chain Alpha-Keto Acid Dehydrogenase Complex, E3 Component, Lipoamide Reductase, Lipoamide Dehydrogenase, LAD, Lipoyl Dehydrogenase, Dihydrolipoyl Dehydrogenase, Diaphorase, Glycine Cleavage System L Protein, GCSL,
  • Ciliary Dyskinesia, Primary, 1
    OMIM # 244400
    CILD1, PCD, Ciliary Dyskinesia, Primary, 1, with or without Situs Inversus, Immotile Cilia Syndrome, ICS, Polynesian Bronchiectasis, Kartagener Syndrome, Dextrocardia, Bronchiectasis, and Sinusitis, Siewert Syndrome
  • Radial Spoke Head 9, Chlamydomonas, Homolog of
    OMIM # 612648
    RSPH9
  • Vici Syndrome
    OMIM # 242840
    VICIS, Immunodeficiency with Cleft Lip/Palate, Cataract, Hypopigmenation, and Absent Corpus Callosum
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