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CTGA Database Listing
Arab Genomic Studies
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  • Transfer RNA, Mitochondrial, Alanine
    OMIM # 590000
    tRNA-ALA, Mitochondrial
  • Spinocerebellar Ataxia 15
    OMIM # 606658
    SCA15, Spinocerebellar Ataxia 16, SCA16,
  • Inositol 1,4,5-Triphosphate Receptor, Type 1
    OMIM # 147265
    ITPR1, IP3R, IP3R1
  • Glycogen Storage Disease I
    OMIM # 232200
    GSD I, GSD1, Glycogen Storage Disease Ia, GSD1A, Von Gierke Disease, Hepatorenal Form of Glycogen Storage Disease, Glucose-6-Phosphatase Deficiency, Hepatorenal Glycogenosis, Glucose-6-Phosphatase, Catalytic, G6PC, Glucose-6-Phosphatase, Catalytic, 1, G6PC1, G6PT
  • Glucose-6-Phosphatase, Catalytic
    OMIM # 613742
    G6PC, Glucose-6-Phosphatase, Catalytic, 1, G6PC1, G6PT
  • Combined Oxidative Phosphorylation Deficiency 31
    OMIM # 617228
    COXPD31
  • Mitochondrial Intermediate Peptidase
    OMIM # 602241
    MIPEP
  • Myasthenic Syndrome, Congenital, 2A, Slow-Channel
    OMIM # 616313
    CMS2A
  • CHRNB1
    OMIM # 100710
    CHRNB, Acetylcholine Receptor, Muscle, Beta Subunit; ACHRB
  • Cardiofaciocutaneous Syndrome
    OMIM # 115150
    CFC Syndrome
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