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CTGA Database Listing
Arab Genomic Studies
Records found: 2565 Sort by:
  • Thyroid Carcinoma, Familial Medullary
    OMIM # 155240
    MTC, FMTC, MTC1
  • Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa
    OMIM # 155145
    Pai Syndrome
  • Mastocytosis, cutaneous
    OMIM # 154800
    MASTC, Mastocytosis, Maculopapular Cutaneous, Urticaria Pigmentosa, Mastocytosis, Diffuse Cutaneous,
  • Deafness, Autosomal Recessive 84B
    OMIM # 614944
    DFNB84B
  • Otogelin-Like Protein
    OMIM # 614925
    OTOGL, Chromosome 12 Open Reading Frame 64, C12ORF64
  • Marfan Syndrome
    OMIM # 154700
    MFS, Marfan Syndrome, Type I, MFS1
  • Treacher Collins Syndrome 1
    OMIM # 154500
    TCS1, Treacher Collins-Franceschetti Syndrome, TCOF, Treacher Collins Syndrome, TCS, Mandibulofacial Dysostosis, MFD1
  • Macroglobulinemia, Waldenstrom, Susceptibility To, 1
    OMIM # 153600
    WM1, Macroglobulinemia, Waldenstrom, Somatic
  • Systemic Lupus Erythematosus
    OMIM # 152700
    SLE, Excess Lymphocyte Low Molecular Weight DNA, Excess LMW-DNA
  • Apolipoprotein(a)
    OMIM # 152200
    LPA, Lipoprotein(a), Lp(a), Lipoprotein Types--Lp System Lp(a) Hyperlipoproteinemia, Sinking Pre-Beta-Lipoprotein, SPB, Lipoprotein(a) Deficiency, Congenital, Lp(a) Deficiency, Congenital, Coronary Artery Disease, Susceptibility to
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