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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • Neurofibromatosis, Type I
    OMIM # 162200
    NF1, Neurofibromatosis, von Recklinghausen Disease, Neurofibromin, Neurofibromatosis, Type I with Leukemia, Neurofibromatosis, Type I with Glioma, NF1 Microdeletion Syndrome, NF1 Microduplication Syndrome
  • Mental Retardation, Autosomal Dominant 13
    OMIM # 614563
    MRD13, Mental Retardation, Autosomal Dominant 13, with Neuronal Migration Defects
  • Dynein, Cytoplasmic 1, Heavy Chain 1
    OMIM # 600112
    DYNC1H1, DNCH1, Dynein, Cytoplasmic-Like, DNCL, DNECL, Dynein Heavy Polypeptide, Cytoplasmic, DHC1, DHC1A, DNCHC1
  • p21 Protein-Aactivated Kinase 3
    OMIM # 300142
    PAK3, p21 CDC42/RAC1-Activated Kinase 3, Oligophrenin 3, OPHN3,
  • Mental Retardation, X-Linked 30
    OMIM # 300558
    MRX30, Mental Retardation, X-Linked 47, MRX47
  • FRAS1 Gene
    OMIM # 607830
    FRAS1, KIAA1500,
  • Fraser Syndrome 1
    OMIM # 219000
    FRASRS1, Fraser Syndrome, Cryptophthalmos with Other Malformations, Cryptophthalmos-Syndactyly Syndrome
  • Cystinosin
    OMIM # 606272
    CTNS
  • Cystinosis, Nephropathic
    OMIM # 219800
    CTNS, Lysosomal Cystine Transport Protein, Defect of, Cystinosin, Defect of, Cystinosis, Infantile Nephropathic , Cystinosis, Atypical Nephropathic
  • 3-@Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase
    OMIM # 607764
    HSD3B7
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