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CTGA Database Listing
Arab Genomic Studies
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  • Basal Cell Nevus Syndrome
    OMIM # 109400
    BCNS, Nevoid Basal Cell Carcinoma Syndrome, NBCCS, Multiple Basal Cell Nevi, Odontogenic Keratocysts, and Skeletal Anomalies, Fifth Phacomatosis, Gorlin Syndrome, Gorlin-Goltz Syndrome
  • Frank-Ter Haar Syndrome
    OMIM # 249420
    FTHS, Ter Haar Syndrome, Borrone Dermatocardioskeletal Syndrome, Melnick-Needles Syndrome, Autosomal Recessive,
  • SH3 and PX Domains-Containing Protein 2B
    OMIM # 613293
    SH3PXD2B, Tyrosine Kinase Substrate With 4 SH3 Domains, TKS4, KIAA1295,
  • Fever, Familial Lifelong Persistent
    OMIM # 228400
  • Atrial Septal Defect 1
    OMIM # 108800
    ASD1, Atrial Septal Defect, Primum Type, ASD I, Atrial Septal Defect, Secundum Type, ASD II
  • Atherosclerosis Susceptibility
    OMIM # 108725
    ATHS, Atherogenic Lipoprotein Phenotype, ALP
  • 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
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