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CTGA Database Listing
Arab Genomic Studies
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  • 17-Beta Hydroxysteroid Dehydrogenase III Deficiency
    OMIM # 264300
    17-Ketosteroid Reductase Deficiency of Testis, 17-KSR Deficiency, Neutral 17-Beta-Hydroxysteroid Oxidoreductase Deficiency, Pseudohermaphroditism, Male, with Gynecomastia, Polycystic Ovarian Disease due to 17-Ketosteroid Reductase Deficiency,
  • Hepatic Venoocclusive Disease with Immunodeficiency
    OMIM # 235550
    VODI
  • Nuclear Body Protein SP110
    OMIM # 604457
    SP110, Speckled, 110-KD , Intracellular Pathogen Resistance 1, Mouse, Homolog of IPR1
  • Cone-Rod Dystrophy 19
    OMIM # 615860
    CORD19
  • Tubulin Tyrosine Ligase-like Family, Member 5
    OMIM # 612268
    TTLL5
  • Transient Receptor Potential Cation Channel, Subfamily M, Member 1
    OMIM # 603576
    TRPM1, Melastatin 1, MLSN1,
  • Night Blindness, Congenital Stationary, Type 1C
    OMIM # 613216
    CSNB1C, CSNB, Complete, Autosomal Recessive,
  • Thiamine-Responsive Megaloblastic Anemia Syndrome
    OMIM # 249270
    TRMA, Thiamine Metabolism Dysfunction Syndrome 1 (Megaloblastic Anemia, Diabetes mellitus, and deafness Type), THMD1, Megaloblastic Anemia, Thiamine-Responsive, with Diabetes Mellitus and Sensorineural Deafness, Rogers Syndrome, Thiamine-Responsive Anemia Syndrome, Thiamine-Responsive Myelodysplasia,
  • Solute Carrier Family 19 (Thiamine Transporter), Member 2
    OMIM # 603941
    SLC19A2, Thiamine Transporter Protein 1, THTR1, THT1
  • Retinal Pigment Epithelium-Specific Protein, 65-kD
    OMIM # 180069
    RPE65
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