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CTGA Database Listing
Arab Genomic Studies
Records found: 2613 Sort by:
  • Spastic Diplegia, Infantile Type
    OMIM # 270600
  • Spastic Paraplegia 23
    OMIM # 270750
    SPG23, Spastic Paraplegia with Pigmentary Abnormalities, Spastic Paraparesis, Vitiligo, Premature Graying, Characteristic Facies, Lison Syndrome,
  • Spastic Paraplegia 5A, Autosomal Recessive
    OMIM # 270800
    SPG5A
  • Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation
    OMIM # 270950
  • Spinocerebellar Ataxia with Dysmorphism
    OMIM # 271270
  • Spinocerebellar Degeneration with Macular Corneal Dystrophy, Congenital Cataracts, and Myopia
    OMIM # 271320
    Bedouin Spastic Ataxia Syndrome
  • Spinocerebellar Degeneration with Slow Eye Movements
    OMIM # 271322
    SDSEM
  • Spondyloepimetaphyseal Dysplasia with Joint Laxity
    OMIM # 271640
    SEMDJL1, SEMDJL
  • Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type
    OMIM # 271665
    SMED, Short Limb-Hand Type, SMED, Type II, Spondylometaepiphyseal Dysplasia, Short Limb-Abnormal Calcification Type, SMED, Short Limb-Abnormal Calcification Type,
  • Canavan Disease
    OMIM # 271900
    Canavan-van Bogaert-Bertrand Disease, Spongy Degeneration of Central Nervous System, Aspartoacylase Deficiency, ASPA Deficiency, ASP Deficiency, Aminoacylase 2 Deficiency, ACY2 Deficiency,
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