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CTGA Database Listing
Arab Genomic Studies
Records found: 2746 Sort by:
  • Beta-Thalassemia
    OMIM # 613985
  • Hemoglobin - Beta Locus
    OMIM # 141900
    HBB
  • Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects
    OMIM # 603642
  • Cutis Laxa, Autosomal Recessive, Type IA
    OMIM # 219100
    ARCL1A, ARCL1, Cutis Laxa, Autosomal Recessive
  • Elastin
    OMIM # 130160
    ELN
  • Fibulin 5
    OMIM # 604580
    FBLN5 , Developmental Arteries and Neural Crest EGF-Like, DANCE
  • Epileptic Encephalopathy, Early Infantile, 1
    OMIM # 308350
    EIEE1, Infantile Spasm Syndrome, X-Linked 1, ISSX1, West Syndrome, X-Linked, Infantile Epileptic-Dyskinetic Encephalopathy, XMESID
  • Tumor Necrosis Factor
    OMIM # 191160
    TNF, Tumor Necrosis Factor, Alpha, TNFA, Cachectin, TNF, Monocyte-Derived, TNF, Macrophage-Derived
  • Pregnancy Loss, Recurrent, Susceptibility to, 1
    OMIM # 614389
    RPRGL1, RPRGL, RPL, Abortion, Spontaneous, Recurrent, Fetal Loss, Recurrent, Susceptibility to, Miscarriage, Recurrent, Embryonic Loss, Recurrent, Stillbirth, Recurrent
  • Inflammatory Bowel Disease 1
    OMIM # 266600
    Regional Enteritis, Crohn Disease, Ulcerative Colitis, Crohn Disease-Associated Growth Failure, Susceptibility to
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