Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2613 Sort by:
  • Revesz Syndrome
    OMIM # 268130
    Exudative Retinopathy with Bone Marrow Failure, Revesz Debuse Syndrome, Bilateral Coats Retinopathy Associated with Aplastic Anaemia and Mild Dyskeratotic Signs, Retinopathy Anemia CNS Anomalies,
  • Myoglobinuria, Acute Recurrent, Autosomal Recessive
    OMIM # 268200
    Myoglobinuria, Familial Paroxysmal Paralytic, Rhabdomyolysis, Acute Recurrent
  • Rhabdomyosarcoma 1
    OMIM # 268210
    RMS1, Rhabdomyosarcoma, Embryonal, 1, RMSE1, Rhabdomyosarcoma Chromosomal Region, RMSCR
  • Rheumatic Fever-Related Antigen
    OMIM # 268240
    Rheumatic Fever, Acute, Susceptibility to
  • Rothmund-Thomson Syndrome
    OMIM # 268400
    RTS, Poikiloderma Atrophicans and Cataract
  • Sandhoff Disease
    OMIM # 268800
    GM2-Gangliosidosis, Type II, Hexosaminidases A and B Deficiency, Sandhoff Disease, Adult Type, Sandhoff Disease, Juvenile Type, Sandhoff Disease, Infantile Type
  • Schizencephaly
    OMIM # 269160
  • Autoimmune Polyendocrine Syndrome, Type II
    OMIM # 269200
    APS2, Schmidt Syndrome , Diabetes Mellitus, Addison Disease, Myxedema, Polyglandular Autoimmune Syndrome, Type II, PGA II, Polyendocrine Autoimmune Syndrome, Type II, APS II,
  • Schneckenbecken Dysplasia
    OMIM # 269250
    Chondrodysplasia, Lethal Neonatal, with Snail-Like Pelvis
  • Lipodystrophy, Congenital Generalized, Type 2
    OMIM # 269700
    CGL2, Berardinelli-Seip Congenital Lipodystrophy Type 2, Seip Syndrome, Berardinelli Syndrome, Lipodystrophy, Total, and Acromegaloid Gigantism, Congenital Lipoatrophic Diabetes, Lipodystrophy, Berardinelli-Seip Congenital Type 2, Brunzell Syndrome, Brunzell Syndrome, BSCL2-Related
  1. <<
  2. ...
  3. 6
  4. 7
  5. 8
  6. 9
  7. 10
  8. 11
  9. 12
  10. 13
  11. 14
  12. 15
  13. 16
  14. 17
  15. ...
  16. >>