Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2310 Sort by:
  • Histone Cell Cycle Regulation Defective, S. Cerevisiae, Homolog of, A
    OMIM # 600237
    HIRA
  • Cyclin-Dependent Kinase-Like 5
    OMIM # 300203
    CDKL5, Serine/Threonine Protein Kinase 9, STK9
  • Epileptic Encephalopathy, Early Infantile, 2
    OMIM # 300672
    EIEE2, Infantile Spasm Syndrome, X-Linked 2, ISSX2
  • Cholestasis, Benign Recurrent Intrahepatic, 1
    OMIM # 243300
    BRIC1, Summerskill Syndrome
  • ATPase, Class I, Type 8B, Member 1
    OMIM # 602397
    ATP8B1, FIC Gene 1, FIC1
  • Titin
    OMIM # 188840
    TTN, Connectin
  • Cardiomyopathy, Dilated, 1G
    OMIM # 604145
    CMD1G
  • Forkhead Box G1
    OMIM # 164874
    FOXG1, Forkhead Box G1B, FOXG1B, Forkhead-Like 1, FKHL1, Oncogene QIN, Brain Factor 1, BF1
  • Rett Syndrome, Congenital Variant
    OMIM # 613454
    FOXG1 Syndrome
  • Glycine Receptor, Alpha-1 Subunit
    OMIM # 138491
    GLRA1
  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. >>