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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • Obscurin-Like 1
    OMIM # 610991
    OBSL1, KIAA0657
  • Three M Syndrome 2
    OMIM # 612921
    3M2, 3M Syndrome 2
  • Three M Syndrome 1
    OMIM # 273750
    3M1, 3M Syndrome, Le Merrer Syndrome, Dolichospondylic Dysplasia, Gloomy Face Syndrome
  • Pyrroline-5-Carboxylate Reductase 1
    OMIM # 179035
    PYCR1
  • Cutis Laxa, Autosomal Recessive, Type IIB
    OMIM # 612940
    ARCL2B, Cutis Laxa with Progeroid Features,
  • Familial Mediterranean Fever Gene
    OMIM # 608107
    MEFV, Pyrin, Marenostrin,
  • Immunodeficiency 15B
    OMIM # 615592
    IMD15B
  • Inhibitor of Nuclear Factor Kappa-B Kinase, Subunit Beta
    OMIM # 603258
    IKBKB, Inhibitor of Kappa Light Chain Gene Enhancer in B Cells, Kinase of, Beta, Nuclear Factor of Kappa Light Chain Gene Enhancer in B Cells Inhibitor, Kinase of, Beta, IKK-Beta, IKKB, I-Kappa-B Kinase, IKK2
  • Rothmund-Thomson Syndrome
    OMIM # 268400
    RTS, Poikiloderma Atrophicans and Cataract
  • Cerebral Palsy, Spastic Quadriplegic 3
    OMIM # 617008
    CPSQ3
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