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CTGA Database Listing
Arab Genomic Studies
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  • Arteriovenous Malformations of the Brain
    OMIM # 108010
    BAVM, Cerebral Arteriovenous Malformations, Intracranial Hemorrhage in Brain Arteriovenous Malformations, Susceptibility to
  • Apnea, Obstructive Sleep
    OMIM # 107650
    OSA, Obstructive Sleep Apnea Syndrome, OSAS, Sleep Apnea/Hypopnea Syndrome, SAHS, OSAHS
  • Aplasia Cutis Congenita, Nonsyndromic
    OMIM # 107600
    ACC, Congenital Defect of Skull and Scalp, Scalp Defect, Congenital
  • Antiphospholipid Syndrome, Familial
    OMIM # 107320
    APS, Lupus Anticoagulant, Familial, Hughes Syndrome
  • Total Anomalous Pulmonary Venous Return 1
    OMIM # 106700
    TAPVR1, Anomalous Pulmonary Venous Return, APVR, Scimitar Syndrome, Scimitar Anomaly
  • Spondyloarthropathy, Susceptibility to, 1
    OMIM # 106300
    SPDA1, Spondyloarthropathy, Ankylosing Spondylitis, Susceptibility to, Ankylosing Spondylitis, AS, Marie-Strumpell Spondylitis, Bechterew Syndrome, Poker Back, Rheumatoid Spondyliti
  • Aniridia
    OMIM # 106210
    AN, Aniridia II, AN2
  • Angioedema, Hereditary
    OMIM # 106100
    HAE, Angioneurotic Edema, Hereditary, HANE, C1 Esterase Inhibitor, Deficiency of, Angioedema, Hereditary, Type I, Angioedema, Hereditary, Type II
  • Angelman Syndrome
    OMIM # 105830
    AS, Happy Puppet Syndrome
  • Diamond-Blackfan Anemia 1
    OMIM # 105650
    DBA1, Blackfan-Diamond Syndrome, BDS, Anemia, Congenital Hypoplastic, of Blackfan and Diamond, Anemia, Congenital Erythroid Hypoplastic, Red Cell Aplasia, Pure, Hereditary, Aregenerative Anemia, Chronic Congenital, Erythrogenesis Imperfecta, AASE-Smith Syndrome II, AASE Syndrome
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