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CTGA Database Listing
Arab Genomic Studies
Records found: 2613 Sort by:
  • Knobloch Syndrome 1
    OMIM # 267750
    KNO1, KNO, Retinal Detachment and Occipital Encephalocele
  • Retinitis Pigmentosa
    OMIM # 268000
    RP
  • Retinopathy, Pigmentary, and Mental Retardation
    OMIM # 268050
    Mirhosseini-Holmes-Walton Syndrome,
  • Enhanced S-Cone Syndrome
    OMIM # 268100
    ESCS, Goldmann-Favre Syndrome, Retinoschisis with Early Hemeralopia, Favre Hyaloideoretinal Degeneration
  • 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
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