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CTGA Database Listing
Arab Genomic Studies
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  • 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
  • Pilonidal Sinus
    OMIM # 173000
    PNS, Jeep Rider's Disease,
  • Pneumothorax, Primary Spontaneous
    OMIM # 173600
    PSP
  • Piebald Trait
    OMIM # 172800
    PBD, Piebaldism
  • Multiple Endocrine Neoplasia, Type IIA
    OMIM # 171400
    MEN2A, Pheochromocytoma and Amyloid-Producing Medullary Thyroid Carcinoma, PTC Syndrome, Sipple Syndrome, Thyroid Carcinoma, Familial Medullary
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