Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2310 Sort by:
  • Centrosomal Protein, 290-KD
    OMIM # 610142
    CEP290, Antigen Identified By Monoclonal Antibody 3H11, 3H11AG, KIAA0373, Nephrocystin 6, NPHP6, BBS14 Gene
  • Renal-Hepatic-Pancreatic Dysplasia 2
    OMIM # 615415
    RHPD2
  • Meckel Syndrome, Type 11
    OMIM # 615397
    MKS11
  • 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
  1. <<
  2. ...
  3. 11
  4. 12
  5. 13
  6. 14
  7. 15
  8. 16
  9. 17
  10. 18
  11. 19
  12. 20
  13. 21
  14. 22
  15. ...
  16. >>