Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2887 Sort by:
  • Peripheral Neuropathy, Autosomal Recessive, with or without Impaired Intellectual Development
    OMIM # 618124
    PNRIID
  • Minichromosome Maintenance 3-Associated Protein
    OMIM # 603294
    MCM3AP, MCM3-Associated Protein, 80-KD, MAP80, Germinal Center-Associated Nuclear Protein, GANP
  • PMS1 Homolog 2, Mismatch Repair System Component
    OMIM # 600259
    PMS2, Postmeiotic Segregation Increased, S. Cerevisiae, 2, Mismatch Repair Gene PMSL2, PMSL2
  • Retinitis Pigmentosa 38
    OMIM # 613862
    RP38, Rod-Cone Dystrophy, Childhood-Onset
  • MER Tyrosine Kinase Protooncogene
    OMIM # 604705
    MERTK
  • Cyclin-Dependent Kinase Inhibitor 2A
    OMIM # 600160
    CDKN2A, CDKN2, CDK4 Inhibitor, Multiple Tumor Suppressor 1, MTS1, TP16, p16(INK4), p16(INK4A), p14(ARF)
  • Leber Congenital Amaurosis 7
    OMIM # 613829
    LCA7,
  • Cone-Rod Homeobox-Containing Gene
    OMIM # 602225
    CRX,
  • FANCG Gene
    OMIM # 602956
    FANCG, X-Ray Repair, Complementing Defective, in Chinese Hamster, 9, XRCC9,
  • Fanconi Anemia, Complementation Group I
    OMIM # 609053
    FANCI
  1. <<
  2. 1
  3. 2
  4. 3
  5. 4
  6. 5
  7. 6
  8. 7
  9. 8
  10. 9
  11. 10
  12. 11
  13. 12
  14. 13
  15. ...
  16. >>