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CTGA Database Listing
Arab Genomic Studies
Records found: 2535 Sort by:
  • Neutropenia, Chronic Familial
    OMIM # 162700
    Leukopenia, Benign Familial
  • Multiple Endocrine Neoplasia, Type IIB
    OMIM # 162300
    MEN2B, MEN IIB, Neuromata, Mucosal, with Endocrine Tumors, Wagenmann-Froboese Syndrome, Multiple Endocrine Neoplasia, Type III, MEN3, Mucosal Neuroma Syndrome
  • 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
  • Schwannomatosis 1
    OMIM # 162091
    Neurilemmomatosis, Congenital Cutaneous, Neurofibromatosis II, NF II
  • Nemaline Myopathy 3
    OMIM # 161800
    NEM3, Myopathy, Actin, Congenital, with Excess of Thin Myofilaments, Nemaline Myopathy 3, with Intranuclear Rods, Myopathy, Actin, Congenital, with Cores
  • Cardiomyopathy, Dilated, with Woolly Hair, Keratoderma, and Tooth Agenesis
    OMIM # 615821
    DCWHKTA, Carvajal Syndrome, Keratoderma with Woolly Hair
  • Infantile Liver Failure Syndrome 2
    OMIM # 616483
    ILFS2
  • Neuroblastoma-Amplified Sequence
    OMIM # 608025
    NBAS, Neuroblastoma-Amplified Gene , NAG
  • Dystrophia Myotonica 1
    OMIM # 160900
    DM1, Dystrophia Myotonica, DM, Myotonic Dystrophy 1, Steinert Disease, Steinert Myotonic Dystrophy
  • Myopia 2, Autosomal Dominant
    OMIM # 160700
    Myopia 2, MYP2, Nearsightedness
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