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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • 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
  • Adducin 3
    OMIM # 601568
    ADD3, Adducin, Gamma, Adducin-Like, ADDL
  • Myasthenic Syndrome, Congenital, 10
    OMIM # 254300
    CMS10, Myasthenia, Limb-Girdle, Familial, LGM, Congenital Myasthenic Syndrome Type Ib, CMS1B, CMS Ib, Myasthenic Myopathy
  • Downstream of Tyrosine Kinase 7
    OMIM # 610285
    DOK7, Chromosome 4 Open Reading Frame 25, C4ORF25
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