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CTGA Database Listing
Arab Genomic Studies
Records found: 2791 Sort by:
  • Cardiofaciocutaneous Syndrome 1
    OMIM # 115150
    CFC1, CFC Syndrome, CFCS,
  • Lung Cancer
    OMIM # 211980
    Alveolar Cell Carcinoma, Adenocarcinoma of Lung, Non Small Cell Lung Cancer, Lung Cancer, Protection Against
  • Chromodomain Helicase DNA-Binding Protein 7
    OMIM # 608892
    CHD7, KIAA1416
  • ATP-Binding Cassette, Subfamily B, Member 6
    OMIM # 605452
    ABCB6
  • Microphthalmia, Isolated, With Coloboma 7
    OMIM # 614497
    MCOPCB7
  • Cone-Rod Dystrophy 3
    OMIM # 604116
    CORD3
  • ATP-Binding Cassette, Subfamily A, Member 4
    OMIM # 601691
    ABCA4, ATP-Binding Cassette Transporter, Retina-Specific, ABCR, ABC Transporter, Retina-Specific, Photoreceptor RIM Protein, RMP,
  • Usher Syndrome, Type IIA
    OMIM # 276901
    USH2A
  • Retinitis Pigmentosa 39
    OMIM # 613809
    RP39
  • USH2A gene
    OMIM # 608400
    USH2A, Usherin, USH2, US2
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