Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2247 Sort by:
  • Meckel Syndrome, Type 6
    OMIM # 612284
    MKS6
  • Nephrocystin 3
    OMIM # 608002
    NPHP3
  • PKHD1 Gene
    OMIM # 606702
    PKHD1, Fibrocystin, FCYT, Polyductin, Polycystic Kidney and Hepatic Disease 1 Gene
  • Obsessive-Compulsive Disorder
    OMIM # 164230
    OCD
  • Eukaryotic Translation Initiation Factor 2B, Subunit 1
    OMIM # 606686
    EIF2B1, Eukaryotic Translation Initiation Factor 2B, Alpha, EIF2B-Alpha
  • Joubert Syndrome 24
    OMIM # 616654
    JBTS24
  • B9 Domain-Containing Protein 1
    OMIM # 614144
    B9D1, MKS1-Related Protein 1 , MKSR1
  • Meckel Syndrome, Type 9
    OMIM # 614209
    MKS9
  • Joubert Syndrome 9
    OMIM # 612285
    JBTS9
  • RPGRIP1-Like
    OMIM # 610937
    RPGRIP1L, Nephrocystin 8, NPHP8, KIAA1005
  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. >>