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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • 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
  • Vasculopathy, Retinal, with Cerebral Leukodystrophy
    OMIM # 192315
    RVCL, Cerebroretinal Vasculopathy, Hereditary, CRV, Retinopathy, Vascular, with Cerebral and Renal Involvement and Raynaud and Migraine Phenomena
  • 3-Prime Repair Exonuclease 1
    OMIM # 606609
    TREX1, DNase III
  • Periaxin
    OMIM # 605725
    PRX
  • Abelson Helper Integration Site 1
    OMIM # 608894
    AHI1, Jouberin,
  • Joubert Syndrome 3
    OMIM # 608629
    JBTS3
  • Xeroderma Pigmentosum, Complementation Group G
    OMIM # 278780
    XPG, XP, Group G, XPGC, Xeroderma Pigmentosum VII, XP7, Xeroderma Pigmentosum, Type G/Cockayne Syndrome, XPG/CS, Cerebrooculofacioskeletal Syndrome, COFS3
  • Excision-Repair, Complementing Defective, in Chinese Hamster, 5
    OMIM # 133530
    ERCC5, ERCM2, UV Damage, Excision Repair of, UV-135; UVDR, Ultraviolet Sensitivity, Mouse, Complementation of, RAD2, Yeast, Homolog of, Xeroderma Pigmentosum, Group G Correcting Protein; XPGC, XPG, Xeroderma Pigmentosum/Cockayne Syndrome Complex, XPG/CS,
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