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CTGA Database Listing
Arab Genomic Studies
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  • Cerebroretinal Microangiopathy with Calcifications and Cysts
    OMIM # 612199
    CRMCC, Leukoencephalopathy, Brain Calcifications, and Cysts, LCC, Coats Plus Syndrome, Labrune Syndrome
  • Congenital Disorder of Glycosylation, Type In
    OMIM # 612015
    CDG1N, CDG In, CDGIn,
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
    OMIM # 611938
    CPVT2, Ventricular Tachycardia, Stress-Induced Polymorphic, VTSIP,
  • Cardiomyopathy, Dilated, 2A
    OMIM # 611880
    Cardiomyopathy, Dilated, Autosomal Recessive, Cardiomyopathy, Congestive, Autosomal Recessive
  • Kawasaki Disease
    OMIM # 611775
    KD, Mucocutaneous Lymph Node Syndrome, Infantile Polyarteritis
  • Renal Tubular Acidosis, Distal, with Hemolytic Anemia
    OMIM # 611590
    RTA, Distal, Autosomal Recessive, with Hemolytic Anemia
  • Joubert Syndrome 7
    OMIM # 611560
    JBTS7
  • Renal Tubular Acidosis, Distal, with Nephrocalcinosis, Short Stature, Mental Retardation, and Distinctive Facies
    OMIM # 611555
  • Cataract 17, Multiple Types
    OMIM # 611544
    CTRCT17, Cataract, Congenital Nuclear, Autosomal Recessive 3, CATCN3
  • Spastic Paraplegia 18, Autosomal Recessive
    OMIM # 611225
    SPG18, Intellectual Disability, Motor Dysfunction, and Joint Contractures, IDMDC,
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