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CTGA Database Listing
Arab Genomic Studies
Records found: 2441 Sort by:
  • Cystinuria
    OMIM # 220100
    Cystinuria, Type I, Cystinuria, Type I, Formerly, CSNU1, Formerly, Cystinuria, Type II, Formerly, Cystinuria, Type III, Formerly, CSNU3, Formerly, Cystinuria, Type Non-I, Formerly, Cystinuria, Type A , Cystinuria, Type B, Cystinuria, Type A/B,
  • Deafness, Autosomal Recessive 9
    OMIM # 601071
    DFNB9, Neurosensory Nonsyndromic Recessive Deafness 9, NSRD9, Auditory Neuropathy, Autosomal Recessive 1, AUNB1, Auditory Neuropathy, Nonsyndromic Recessive, NSRAN, Auditory Neuropathy, Nonsyndromic Recessive, Temperature-Sensitive
  • Epileptic Encephalopathy, Early Infantile, 38
    OMIM # 617020
    EIEE38
  • 3-@Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase (*)
    OMIM # 607764
    HSD3B7
  • Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia due to
    OMIM # 237300
    Carbamoyl Phosphate Synthetase I Deficiency, CPS I Deficiency,
  • Carbamoyl Phosphate Synthetase I
    OMIM # 608307
    CPS1, Venoocclusive Disease after Bone Marrow Transplantation, Susceptibility to
  • KIF5C
    OMIM # 604593
    Kinesin, Heavy Chain, Neuron-Specific, 2, NKHC2
  • SLAIN Motif Family, Member 2
    OMIM # 610492
    SLAIN2, KIAA1458
  • Sirtuin 2
    OMIM # 604480
    SIRT2
  • SIAH E3 Ubiquitin Protein Ligase Family, Member 1
    OMIM # 602212
    SIAH1, Seven in Absentia, Drosophila, Homolog of, 1
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