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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • AT-Rich Interaction Domain-Containing Protein 1B
    OMIM # 614556
    ARID1B, ARID-Containing Protein, BAF-Associated Factor, BAF250B, ELD/OSA1, KIAA1235
  • Epidermolysis Bullosa Simplex with Pyloric Atresia
    OMIM # 612138
    EBSPA, EBS with Pyloric Atresia
  • Plectin
    OMIM # 601282
    PLEC, PLEC1, PCN, PLTN
  • ALMS1 Gene
    OMIM # 606844
    ALMS1, KIAA0328,
  • Cyclic Nucleotide-Gated Channel, Alpha-3
    OMIM # 600053
    CNGA3, Cone Photoreceptor cGMP Channel, Cyclic Nucleotide-Gated Channel, Olfactory, 3, CNG3,
  • Epidermolysis Bullosa Simplex with Muscular Dystrophy
    OMIM # 226670
    EBS-MD, Epidermolysis Bullosa Simplex and Limb-Girdle Muscular Dystrophy, MD-EBS, MDEBS
  • Lipodystrophy, Congenital Generalized, Type 2
    OMIM # 269700
    CGL2, Berardinelli-Seip Congenital Lipodystrophy Type 2, Seip Syndrome, Berardinelli Syndrome, Lipodystrophy, Total, and Acromegaloid Gigantism, Congenital Lipoatrophic Diabetes, Lipodystrophy, Berardinelli-Seip Congenital Type 2, Brunzell Syndrome, Brunzell Syndrome, BSCL2-Related
  • ATP-Binding Cassette, Subfamily A, Member 4
    OMIM # 601691
    ABCA4, ATP-Binding Cassette Transporter, Retina-Specific, ABCR, ABC Transporter, Retina-Specific, Photoreceptor RIM Protein, RMP,
  • Stargardt Disease 1
    OMIM # 248200
    STGD1, STGD, Macular Degeneration, Juvenile, Macular Dystrophy with Flecks, Type 1, Fundus Flavimaculatus, FFM, Retinal Dystrophy, Early-Onset Severe
  • Neurofibromin 1
    OMIM # 613113
    Neurofibromin
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