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CTGA Database Listing
Arab Genomic Studies
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  • 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
  • Interleukin 10 Receptor, Alpha
    OMIM # 146933
    IL10RA, Interleukin 10 Receptor, IL10R, IL10R1,
  • Leukodystrophy, Hypomyelinating, 7, with or without Oligodontia and/or Hypogonadotropic Hypogonadism
    OMIM # 607694
    Leukoencephalopathy, Hypomyelinating, with Ataxia and Delayed Dentition, Ataxia, Delayed Dentition, and Hypomyelination, ADDH, Leukodystrophy, Hypomyelinating, with Hypodontia and Hypogonadotropic Hypogonadism, 4H Syndrome
  • Polymerase IIII, RNA, Subunit A
    OMIM # 614258
    POLR3A, RNA Polymerase III, Subunit C1, RPC1, RNA Polymerase III, 155-KD Subunit, RPC155
  • Transcription Factor For Immunoglobulin Heavy-Chain Enhancer 3
    OMIM # 314310
    TFE3, TFE3/ASPSCR1 Fusion Gene, TFE3/PRCC Fusion Gene, TFE3/SFPQ Fusion Gene, TFE3/CLTC Fusion Gene
  • Alveolar Soft Part Sarcoma Chromosome Region, Candidate 1
    OMIM # 606236
    ASPSCR1, Alveolar Soft Part Sarcoma Locus, ASPL, Tether Containing UBX Domain For GLUT4, TUG, ASPSCR1/TFE3 Fusion Gene
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