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CTGA Database Listing
Arab Genomic Studies
Records found: 2613 Sort by:
  • Postmeiotic Segregation Increased, S. Cerevisiae, 2
    OMIM # 600259
    PMS2, Mismatch Repair Gene PMSL2, PMSL2
  • Mismatch Repair Cancer Syndrome
    OMIM # 276300
    MMRCS, Mismatch Repair Deficiency, MMR Deficiency, Childhood Cancer Syndrome, Brain Tumor-Polyposis Syndrome 1, BTPS1, BTP1 Syndrome, Turcot Syndrome
  • Myotubularin-Related Protein 2
    OMIM # 603557
    MTMR2
  • Charcot-Marie-Tooth Disease, Type 4B1
    OMIM # 601382
    CMT4B1, Charcot-Marie-Tooth Disease, With Focally Folded Myelin Sheaths, Autosomal Recessive, Type 4B1, Charcot-Marie-Tooth Neuropathy, Type 4B1, Charcot-Marie-Tooth Disease, Type 4B, CMT4B
  • Charcot-Marie-Tooth Disease, Demyelinating, Type 4F
    OMIM # 614895
    CMT4F
  • Major Histocompatibility Complex, Class I, C
    OMIM # 142840
    HLA-C, HLA-C Histocompatibility Type
  • Major Histocompatibility Complex, Class I, B
    OMIM # 142830
    HLA-B, HLA-B Histocompatibility Type
  • Major Histocompatibility Complex, Class I, A
    OMIM # 142800
    HLA-A, HLA-A Histocompatibility Type
  • Transcription Factor 7-Like 2
    OMIM # 602228
    TCF7L2, T-Cell Transcription Factor 4, TCF4
  • Diabetes Mellitus, Noninsulin-Dependent
    OMIM # 125853
    NIDDM, Diabetes Mellitus, Type II, T2D, Noninsulin-Dependent Diabetes Mellitus, Maturity-Onset Diabetes, Insulin Resistance, Susceptibility to
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