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CTGA Database Listing
Arab Genomic Studies
Records found: 2829 Sort by:
  • Thymidine Kinase, Mitochondrial
    OMIM # 188250
    TK2
  • Myosin VIIA
    OMIM # 276903
    MYO7A, Myosin, Unconventional, Family VII, Member A, MYU7A,
  • Split-Hand/Foot Malformation with Long Bone Deficiency 2
    OMIM # 610685
    SHFLD2, Cleft Hand and Absent Tibia, Aplasia of Tibia with Ectrodactyly, Ectrodactyly with Aplasia of Long Bones, Tibial Aplasia with Split-Hand/Split Foot Deformity
  • Joubert Syndrome 16
    OMIM # 614465
    JBTS16
  • Transmembrane Protein 138
    OMIM # 614459
    TMEM138
  • Deafness, Autosomal Recessive 2
    OMIM # 600060
    DFNB2, Neurosensory Nonsyndromic Recessive Deafness 2 , NSRD2,
  • 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
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