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CTGA Database Listing
Arab Genomic Studies
Records found: 2572 Sort by:
  • Hypertrophic Neuropathy of Dejerine-Sottas
    OMIM # 145900
    Dejerine-Sottas Syndrome , DSS, Hereditary Motor and Sensory Neuropathy Type III, HMSN3, Dejerine-Sottas Neuropathy , DSN, Charcot-Marie-Tooth Disease, Demyelinating, Type 3, CMT3
  • Periaxin
    OMIM # 605725
    PRX
  • Jagged 1
    OMIM # 601920
    JAG1, JAGL1,
  • Alagille Syndrome 1
    OMIM # 118450
    ALGS1, Alagille Syndrome, ALGS, Alagille-Watson Syndrome, AWS, Cholestasis with Peripheral Pulmonary Stenosis, Arteriohepatic Dysplasia, AHD, Hepatic Ductular Hypoplasia, Syndromatic
  • Behçet Syndrome
    OMIM # 109650
    Behçet Disease, BD
  • Major Histocompatibility Complex, Class I, B
    OMIM # 142830
    HLA-B, HLA-B Histocompatibility Type, Abacavir Hypersensitivity, Susceptibility to, Synovitis, Chronic, Susceptibility to
  • Intercellular Adhesion Molecule 1
    OMIM # 147840
    ICAM1, CD54, Surface Antigen of Activated B Cells, BB2, BB2, Antigen Identified by Monoclonal Antibody BB2
  • Atrial Septal Defect 1
    OMIM # 108800
    ASD1, Atrial Septal Defect, Primum Type, ASD I, Atrial Septal Defect, Secundum Type, ASD II
  • Spondyloarthropathy, Susceptibility to, 1
    OMIM # 106300
    SPDA1, Spondyloarthropathy, Ankylosing Spondylitis, Susceptibility to, Ankylosing Spondylitis, AS, Marie-Strumpell Spondylitis, Bechterew Syndrome, Poker Back, Rheumatoid Spondylitis
  • Amyloidosis, Primary Localized Cutaneous, 1
    OMIM # 105250
    PLCA1, Amyloidosis, Primary Cutaneous, 1, PCA1, PCA, Lichen Amyloidosis, Familial, Amyloidosis IX, Amyloidosis, Familial Cutaneous Lichen
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