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CTGA Database Listing
Arab Genomic Studies
Records found: 2791 Sort by:
  • Cone-Rod Dystrophy 13
    OMIM # 608194
    CORD13
  • F-Box and Leucine-Rich Repeat Protein 4
    OMIM # 605654
    FBXL4
  • Mitochondrial DNA Depletion Syndrome 13 (Encephalomyopathic Type)
    OMIM # 615471
    MTDPS13, Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form with Variable Craniofacial Anomalies
  • Mental Retardation, Autosomal Recessive 36
    OMIM # 615286
    MRT36, Intellectual Disability-Strabismus Syndrome,
  • Adenosine Deaminase, tRNA-Specific, 3
    OMIM # 615302
    ADAT3, TAD3, S. cerevisiae, Homolog of , TAD3,
  • Senior-Loken Syndrome 4
    OMIM # 606996
    SLSN4,
  • Nephrocystin 4
    OMIM # 607215
    NPHP4, KIAA0673, Nephroretinin
  • Myosin VIIA
    OMIM # 276903
    MYO7A, Myosin, Unconventional, Family VII, Member A, MYU7A,
  • MER Tyrosine Kinase Protooncogene
    OMIM # 604705
    MERTK
  • Leber Congenital Amaurosis 14
    OMIM # 613341
    LCA14, Retinal Dystrophy, Early-Onset Severe, LRAT-Related, Retinitis Pigmentosa, Juvenile, LRAT-Related,
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