Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2191 Sort by:
  • Activin A Receptor, Type II-Like 1
    OMIM # 601284
    ACVRL1, Activin A Receptor, Type II-Like Kinase 1, ACVRLK1, Activin Receptor-Like Kinase 1, ALK1,
  • Athabaskan Brainstem Dysgenesis Syndrome
    OMIM # 601536
    ABDS, Navajo Brainstem Syndrome, Bosley-Salih-Alorainy Syndrome, BSAS
  • Fibrosis of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement
    OMIM # 600638
    CFEOM3A, FEOM3 Locus,
  • HCLS1-Associated Protein X1
    OMIM # 605998
    HAX1
  • Oculopharyngeal Muscular Dystrophy
    OMIM # 164300
    OPMD, Muscular Dystrophy, Oculopharyngeal,
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
    OMIM # 611938
    CPVT2, Ventricular Tachycardia, Stress-Induced Polymorphic, VTSIP,
  • Anti-Mullerian Hormone Type II Receptor
    OMIM # 600956
    AMHR2, Anti-Mullerian Hormone Receptor, AMHR, Mullerian Inhibiting Substance Type II Receptor, MISR2,
  • Membrane-Type Frizzled-Related Protein
    OMIM # 606227
    MFRP
  • Microphthalmia, Isolated 5
    OMIM # 611040
    MCOP5, Microphthalmia, Posterior, with Retinitis Pigmentosa, Foveoschisis, and Optic Disc Drusen,
  • Protease, Serine, 56
    OMIM # 613858
    PRSS56
  1. <<
  2. ...
  3. 7
  4. 8
  5. 9
  6. 10
  7. 11
  8. 12
  9. 13
  10. 14
  11. 15
  12. 16
  13. 17
  14. 18
  15. ...
  16. >>