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CTGA Database Listing
Arab Genomic Studies
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  • Tyrosyl-tRNA Synthetase 2
    OMIM # 610957
    YARS2, Tyrosyl-tRNA Synthetase, Mitochondrial;, MT-TYRRS
  • Myopathy, Lactoc Acidosis, and Sideroblastic Anemia 2
    OMIM # 613561
    MLASA2
  • Factor XIII, A1 Subunit
    OMIM # 134570
    F13A1, F13A, Fibrin Stabilizing Factor, A Subunit, FSF, A Subunit, Fibrinoligase, Transglutaminase, Plasma,
  • Factor XIII, A Subunit, Deficiency of
    OMIM # 613225
  • Acetylglucosaminyltransferase-Like Protein
    OMIM # 603590
    LARGE1, LARGE, KIAA0609, Like-Glycosyltransferase
  • Muscular Dystrophy-Dystroglycanopathy (Congenital with Mental Retardation), type B, 6
    OMIM # 608840
    MDDGB6, Muscular Dystrophy, LARGE-Related,, Muscular Dystrophy, Type 1D,, MDC1D
  • Mucopolysaccharidosis Type IIIB
    OMIM # 252920
    MPS IIIB, MPS3B, Sanfilippo Syndrome B, N-Acetyl-Alpha-D-Glucosaminidase Deficiency, NAGLU Deficiency, N-Acetylglucosaminidase, Alpha-, NAGLU, N-Acetyl-Alpha-D-Glucosaminidase Polymorphism, NAG Polymorphism,
  • Coagulation Factor XI
    OMIM # 264900
    F11, Factor XI
  • Factor XI Deficiency
    OMIM # 612416
    F11 Deficiency, Plasma Thromboplastin Antecedent Deficiency, PTA Deficiency, Rosenthal Syndrome
  • Mitochondrial DNA Depletion Syndrome 11
    OMIM # 615084
    MTDPS11
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