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CTGA Database Listing
Arab Genomic Studies
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  • Epilepsy, Pyridoxine Dependent
    OMIM # 266100
    EPD, Pyridoxine-Dependent Epilepsy, PDE, Pyridoxine Dependency with Seizures, AASA Dehydrogenase Deficiency
  • Aldehyde Dehydrogenase 7 Family, Member A1
    OMIM # 107323
    ALDH7A1, Antiquitin, ATQ1, Alpha Amino-Adipic Semialdehyde Dehydrogenase, Alpha-AASA Dehydrogenase, AASA Dehydrogenase
  • Cholinergic Receptor, Neuronal Nicotinic, Alpha Polypeptide 4
    OMIM # 118504
    CHRNA4, Acetylcholine Receptor, Neuronal Nicotinic, Alpha-4 Subunit
  • 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
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