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CTGA Database Listing
Arab Genomic Studies
Records found: 2791 Sort by:
  • Interphotoreceptor Matrix Proteoglycan 2
    OMIM # 607056
    IMPG2, SPACRCAN, IPM200
  • Phenylketonuria
    OMIM # 261600
    PKU, Phenylalanine Hydroxylase Deficiency, PAH Deficiency, Oligophrenia Phenylpyruvica, Folling Disease, Hyperphenylalaninemia, Non-PKU Mild, HPA, Non-PKU Mild, Phenylketonuria, Maternal
  • Phenylalanine Hydroxylase
    OMIM # 612349
    PAH
  • Intraflagellar Transport 140, Chlamydomonas, Homolog of
    OMIM # 614620
    IFT140, KIAA0590,
  • Retinitis Pigmentosa 80
    OMIM # 617781
    RP80
  • Cyclic Nucleotide-Gated Channel, Alpha-3
    OMIM # 600053
    CNGA3, Cone Photoreceptor cGMP Channel, Cyclic Nucleotide-Gated Channel, Olfactory, 3, CNG3,
  • Achromatopsia 2
    OMIM # 216900
    ACHM2, Colorblindness, Total, Rod Monochromatism 2, Rod Monochromacy 2, RMCH2,
  • Breast Cancer 1 Gene
    OMIM # 113705
    BRCA1
  • BRCA2 Gene
    OMIM # 600185
    BRCA2, FANCD1 Gene, FANCD1
  • Retinitis Pigmentosa 26
    OMIM # 608380
    RP26
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