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CTGA Database Listing
Arab Genomic Studies
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  • Leri-Weill Dyschondrosteosis
    OMIM # 127300
    LWD, Dyschondrosteosis, DCO, Madelung Deformity
  • Duane Retraction Syndrome 1
    OMIM # 126800
    DURS1, DRS, Duane Syndrome, DUS, Duane Anomaly, Retraction Syndrome
  • Multiple Sclerosis
    OMIM # 126200
    Disseminated Sclerosis, Multiple Sclerosis susceptibility 1, MS1, MS
  • Robinow Syndrome, Autosomal Recessive
    OMIM # 268310
    RRS, Costovertebral Segmentation Defect with Mesomelia, Covesdem Syndrome
  • Receptor Tyrosine Kinase-Like Orphan Receptor 2
    OMIM # 602337
    ROR2, Neurotrophic Tyrosine Kinase, Receptor-Related 2, NTRKR2,
  • Diabetes Mellitus, Noninsulin-Dependent
    OMIM # 125853
    NIDDM, Diabetes Mellitus, Type II, T2D, Noninsulin-Dependent Diabetes Mellitus, Maturity-Onset Diabetes, Insulin Resistance, Susceptibility to,
  • Maturity-Onset Diabetes of the Young, Type II
    OMIM # 125851
    MODY2, MODY, Type 2, MODY, Type II, MODY, Glucokinase-Related
  • Diabetes Insipidus, Nephrogenic, Autosomal
    OMIM # 125800
    Diabetes Insipidus, Nephrogenic, Type II
  • Fabry Disease
    OMIM # 301500
    Angiokeratoma Corporis Diffusum, Anderson-Fabry Disease, Hereditary Dystopic Lipidosis, Alpha-Galactosidase A Deficiency, GLA Deficiency, Ceramide Trihexosidase Deficiency, Fabry Disease, Cardiac Variant
  • Galactosidase, Alpha
    OMIM # 300644
    GLA, Alpha-Galactosidase A, GALA
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