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CTGA Database Listing
Arab Genomic Studies
Records found: 2557 Sort by:
  • Osteogenesis Imperfecta, Type I
    OMIM # 166200
    OI, Type I, OI1, Osteogenesis Imperfecta Tarda, OIT, Osteogenesis Imperfecta with Blue Sclerae, Osteopenic Nonfracture Syndrome
  • Osteogenesis Imperfecta, Type II
    OMIM # 166210
    OI, Type II, OI2, OIC, Osteogenesis Imperfecta Congenita, Osteogenesis Imperfecta Congenita, Perinatal Lethal Form, Vrolik Type of Osteogenesis Imperfecta
  • Zinc Finger Protein 592
    OMIM # 613624
    ZNF592, KIAA0211,
  • Hypophosphatemic Rickets, Autosomal Recessive, 1
    OMIM # 241520
    ARHR1 , ARHR , Hypophosphatemia, Autosomal Recessive , ARHP
  • Dentin Matrix Acidic Phosphoprotein 1
    OMIM # 600980
    DMP1
  • Guanylate Cyclase 2C
    OMIM # 601330
    GUCY2C, Guanylyl Cyclase 2C , GUC2C, Heat-Stable Enterotoxin Receptor
  • Meconium Ileus
    OMIM # 614665
  • Zinc Finger And BTB Domain Containing 24
    OMIM # 614064
    ZBTB24, Zinc Finger Protein 450, POZ (BTB) And AT Hook Containing Zinc Finger 2
  • Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2
    OMIM # 614069
    ICF2
  • Enchondromatosis, Multiple, Ollier Type
    OMIM # 166000
    Osteochondromatosis, Dyschondroplasia, Maffucci Syndrome, Ollier Disease
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