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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • Deafness, Autosomal Recessive 67
    OMIM # 610265
    DFNB67
  • LHFP-Like Protein 5
    OMIM # 609427
    LHFPL5, Tetraspan Membrane Protein of Hair Cell Stereocilia, TMHS
  • NOL1/NOP2/SUN Domain Family, Member 2
    OMIM # 610916
    NSUN2, TRM4, S. Cerevisiae, Homolog of, TRM4, Substrate of AIM1/Aurora Kinase B, SAKI, MYC-Induced SUN Domain-Containing Protein, MISU
  • Mental Retardation, Autosomal Recessive 5
    OMIM # 611091
    MRT5
  • Cullin 7
    OMIM # 609577
    CUL7, KIAA0076
  • Obscurin-Like 1
    OMIM # 610991
    OBSL1, KIAA0657
  • Three M Syndrome 2
    OMIM # 612921
    3M2, 3M Syndrome 2
  • Three M Syndrome 1
    OMIM # 273750
    3M1, 3M Syndrome, Le Merrer Syndrome, Dolichospondylic Dysplasia, Gloomy Face Syndrome
  • Pyrroline-5-Carboxylate Reductase 1
    OMIM # 179035
    PYCR1
  • Cutis Laxa, Autosomal Recessive, Type IIB
    OMIM # 612940
    ARCL2B, Cutis Laxa with Progeroid Features,
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