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CTGA Database Listing
Arab Genomic Studies
Records found: 2791 Sort by:
  • Ceramide Kinase-Like
    OMIM # 608381
    CERKL
  • Nuclear Receptor Subfamily 2, Group E, Member 3
    OMIM # 604485
    NR2E3, Photoreceptor-Specific Nuclear Receptor, PNR
  • Enhanced S-Cone Syndrome
    OMIM # 268100
    ESCS, Goldmann-Favre Syndrome, Retinoschisis with Early Hemeralopia, Favre Hyaloideoretinal Degeneration
  • Retinitis Pigmentosa 37
    OMIM # 611131
    RP37
  • Coenzyme Q8B
    OMIM # 615567
    COQ8B, AARF Domain-Containing Kinase 4, ADCK4
  • Nephrotic Syndrome, Type 9
    OMIM # 615573
    NPHS9
  • Methyltransferase-Like 23
    OMIM # 615262
    METTL23, Chromosome 17 Open Reading Frame 95, C17ORF95,
  • Mental Retardation, Autosomal Recessive 44
    OMIM # 615942
    MRT44
  • Cholinergic Receptor, Nicotinic, Beta Polypeptide 1
    OMIM # 100710
    CHRNB1, CHRNB, Acetylcholine Receptor, Muscle, Beta Subunit; ACHRB
  • Myasthenic Syndrome, Congenital, 2A, Slow-Channel
    OMIM # 616313
    CMS2A
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