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CTGA Database Listing
Arab Genomic Studies
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  • McCune-Albright Syndrome
    OMIM # 174800
    MAS, Albright Syndrome, Polyostotic Fibrous Dysplasia, PFD, POFD,
  • Polydactyly, Preaxial I
    OMIM # 174400
    PPD1, Polydactyly Preaxial , Thumb Polydactyly, Thenar Hypoplasia, Fromont Anomaly
  • Polycystic Liver Disease 1 with or without Kidney Cysts
    OMIM # 174050
    PCLD1
  • Polycystic Kidney Disease 1 with or without Polycystic Liver Disease
    OMIM # 173900
    Polycystic Kidney Disease, PKD, Polycystic Kidney Disease, Adult, APKD, Potter Type III Polycystic Kidney Disease
  • Poland Syndrome
    OMIM # 173800
    Poland Syndactyly, Poland Anomaly, Poland Sequence, Pectoralis Muscle, Absence of, Unilateral Defect of Pectoralis Muscle and Syndactyly of the Hand
  • Mucosa-Associated Lymphoid Tissue Lymphoma Translocation Gene 1
    OMIM # 604860
    MALT1, MLT, Paracaspase,
  • Immunodeficiency 12
    OMIM # 615468
    IMD12
  • Skin Fragility-Woolly Hair Syndrome
    OMIM # 607655
    SFWHS
  • Cardiomyopathy, Dilated, with Woolly Hair, Keratoderma, and Tooth Agenesis
    OMIM # 615821
    DCWHKTA, Carvajal Syndrome, Keratoderma with Woolly Hair
  • Kindler Syndrome
    OMIM # 173650
    KNDLRS, Poikiloderma, Hereditary Acrokeratotic, Bullous Acrokeratotic Poikiloderma of Kindler and Weary, Poikiloderma, Congenital, with Bullae, Weary Type, Poikiloderma of Kindler
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