Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2191 Sort by:
  • Metachromatic Leukodystrophy due to Saposin B Deficiency
    OMIM # 249900
    Metachromatic Leukodystrophy due to Cerebroside Sulfatase Activator Deficiency, Saposin B Deficiency,
  • Polymerase, DNA, Epsilon-2
    OMIM # 602670
    POLE2, DPE2,
  • Weill-Marchesani-like Syndrome
    OMIM # 613195
  • Coiled-Coil and C2 Domains-Containing Protein 2A
    OMIM # 612013
    CC2D2A, KIAA1345,
  • Purine Nucleoside Phosphorylase Deficiency
    OMIM # 613179
    Nucleoside Phosphorylase Deficiency
  • Bernard-Soulier Syndrome
    OMIM # 231200
    BSS, Bleeding Disorder, Platelet-Type, 1, BDPLT1, Platelet Glycoprotein Ib Deficiency, Glycoprotein Ib, Platelet, Deficiency of, Von Willebrand Factor Receptor Deficiency, Bernard-Soulier Syndrome, Type A1, Bernard-Soulier Syndrome, Type B, Bernard-Soulier Syndrome, Type C,
  • Colorblindness, Partial, Deutan Series
    OMIM # 303800
    CBD, Deutan Colorblindness, DCB, Deuteranopia, Green Colorblindness,
  • Colorblindness, Partial, Protan Series
    OMIM # 303900
    CBP, Protanopia, Red Colorblindness,
  • Deoxyribonuclease I-Like 3
    OMIM # 602244
    DNASE1L3
  • Eukaryotic Translation Initiation Factor 2B, Subunit 2
    OMIM # 606454
    EIF2B2, Eukaryotic Translation Initiation Factor 2B, Beta, EIF2B-BETA,
  1. <<
  2. ...
  3. 5
  4. 6
  5. 7
  6. 8
  7. 9
  8. 10
  9. 11
  10. 12
  11. 13
  12. 14
  13. 15
  14. 16
  15. ...
  16. >>