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CTGA Database Listing
Arab Genomic Studies
Records found: 2156 Sort by:
  • Roundabout, Drosophila, Homolog of, 3
    OMIM # 608630
    ROBO3, RB-Inhibiting Gene 1, RBIG1, RIG1
  • Transposition of the Great Arteries, Dextro-Looped
    OMIM # 608808
    DTGA, D-TGA
  • Motor Neuron and Pancreas Homeobox 1
    OMIM # 142994
    MNX1, Homeobox Gene HB9, HLXB9, HB9,
  • Solute Carrier Family 25, Member 42
    OMIM # 610823
    SLC25A42
  • Crumbs, Drosophila, Homolog of, 1
    OMIM # 604210
    CRB1
  • ALG9, S. Cerevisiae, Homolog of
    OMIM # 606941
    Disrupted in Bipolar Disorder 1, DIBD1,
  • Currarino Syndrome
    OMIM # 176450
    Currarino-Triad, Sacral Agenesis Syndrome, Sacral Agenesis, Hereditary, with Presacral Mass, Anterior Meningocele, and/or Teratoma, and Anorectal Malformation, SCRA1,
  • Short-Rib Thoracic Dysplasia 9 with or without Polydactyly
    OMIM # 266920
    SRTD9, Mainzer-Saldino Syndrome, MZSDS, Conorenal Syndrome, Renal Dysplasia, Retinal Pigmentary Dystrophy, Cerebellar Ataxia, and Skeletal Dysplasia,
  • Lysosomal Acid Lipase Deficiency
    OMIM # 278000
    Cholesteryl Ester Storage Disease, CESD, LIPA Deficiency, LAL Deficiency Cholesterol Ester Hydrolase Deficiency, Wolman Disease
  • Glutaric Acidemia I
    OMIM # 231670
    Glutaric Aciduria I, GA I, Glutaryl-CoA Dehydrogenase Deficiency, GDD
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