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CTGA Database Listing
Arab Genomic Studies
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  • Spastic Ataxia 1, Autosomal Dominant
    OMIM # 108600
    SPAX1
  • Stickler Syndrome, Type I
    OMIM # 108300
    STL1, Stickler Syndrome, Vitreous Type 1, Stickler Syndrome, Membranous Vitreous Type, Arthroophthalmopathy, Hereditary Progressive, AOM,
  • Epilepsy, Idiopathic Generalized
    OMIM # 600669
    EIG, Idiopathic Generalized Epilepsy, IGE
  • 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
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