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CTGA Database Listing
Arab Genomic Studies
Records found: 2613 Sort by:
  • Mesoderm Posterior Basic Helix-Loop-Helix Transcription Factor 2
    OMIM # 605195
    MESP2
  • Corneal Endothelial Dystrophy 1, Autosomal Dominant
    OMIM # 121700
    CHED1, Corneal Dystrophy, Congenital Hereditary Endothelial, CHED, Congenital Hereditary Endothelial Dystrophy of Cornea, Maumenee Corneal Dystrophy
  • Arthrogryposis Multiplex Congenita
    OMIM # 108110
    AMC
  • Lipodystrophy, Congenital Generalized, Type 4
    OMIM # 613327
    CGL4, Berardinelli-Seip Congenital Lipodystrophy, Type 4, with Muscular Dystrophy, Lipodystrophy, Berardinelli-Seip Congenital, Type 4, with Muscular Dystrophy,
  • Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 3
    OMIM # 613227
    CAMRQ3, Cerebellar Ataxia and Mental Retardation with or without Quadrupedal Locomotion 3
  • Diarrhea 5, with Tufting Enteropathy, Congenital
    OMIM # 613217
    DIAR5, Enteropathy, Congenital Tufting, CTE, Intestinal Epithelial Cell Dysplasia
  • Night Blindness, Congenital Stationary, Type 1C
    OMIM # 613216
    CSNB1C, CSNB, Complete, Autosomal Recessive,
  • Amelogenesis Imperfecta, Hypomaturation Type, IIA3
    OMIM # 613211
    AI2A3
  • Weill-Marchesani-like Syndrome
    OMIM # 613195
  • Purine Nucleoside Phosphorylase Deficiency
    OMIM # 613179
    Nucleoside Phosphorylase Deficiency
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