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CTGA Database Listing
Arab Genomic Studies
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  • Coagulation Factor II
    OMIM # 176930
    F2, Thrombin, Prothrombin, Factor II
  • Coagulation Factor V
    OMIM # 612309
    F5, Protein C Cofactor, PCCF, Activated Protein C Cofactor, APC Cofactor, Labile Factor, Factor V Leiden
  • Takayasu Arteritis
    OMIM # 207600
    Aortic Arch Syndrome, Young Female Arteritis, Pulseless Disease
  • Argininosuccinic Aciduria
    OMIM # 207900
    Argininosuccinase Deficiency, Argininosuccinate Lyase Deficiency, ASL Deficiency, Argininosuccinic Acid Lyase Deficiency
  • Arthrogryposis, Renal Dysfunction, and Cholestasis 1 (*)
    OMIM # 208085
    ARCS1, ARC Syndrome, ARCS
  • Arthropathy, Progressive Pseudorheumatoid, of Childhood
    OMIM # 208230
    PPAC, Progressive Pseudorheumatoid Arthropathy of Childhood, Spondyloepiphyseal Dysplasia Tarda with Progressive Arthropathy, SEDT-PA, Progressive Pseudorheumatoid Dysplasia, PPD
  • Microcephalic Osteodysplastic Primordial Dwarfism, Type II
    OMIM # 210720
    MOPD II, MOPD2, Osteodysplastic Primordial Dwarfism, Type II, Majewski Osteodysplastic Primordial Dwarfism, Type II
  • Carnitine Deficiency, Systemic Primary
    OMIM # 212140
    CDSP, Systemic Carnitine Deficiency, SCD, Carnitine Deficiency, Systemic, Due To Defect In Renal Reabsorption Of Carnitine, Carnitine Deficiency, Primary, Carnitine Transporter, Plasma-Membrane, Deficiency Of, Carnitine Uptake Defect, CUD
  • Charcot-Marie-Tooth Disease, Type 4A
    OMIM # 214400
    CMT4A, Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive, Type 4A, Charcot-Marie-Tooth Neuropathy, Type 4A
  • Cohen Syndrome
    OMIM # 216550
    COH1, CHH1, Hypotonia Obesity and Prominent Incisors, Pepper Syndrome, CHS1
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