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CTGA Database Listing
Arab Genomic Studies
Records found: 2441 Sort by:
  • Bothnia Retinal Dystrophy
    OMIM # 607475
    Vasterbotten Dystrophy
  • Adiponectin Receptor 1
    OMIM # 607945
    ADIPOR1, CGI45, Progestin and AdipoQ Receptor Family, Member 1, PAQR1,
  • 1-@Acylglycerol-3-Phosphate O-Acyltransferase 2
    OMIM # 603100
    AGPAT2 , Lysophosphatidic Acid Acyltransferase-Beta, LPAAT-Beta,
  • Leukocyte Adhesion Deficiency, Type I
    OMIM # 116920
    LAD, LAD1, Lymphocyte Function-Associated Antigen 1 Immunodeficiency, LFA1 Immunodeficiency
  • Integrin, Beta-2
    OMIM # 600065
    ITGB2, Leukocyte Cell Adhesion Molecule CD18, CD18, Leukocyte-Associated Antigens CD18/11A, CD18/11B, CD18/11C
  • Niemann-Pick Disease, Type B
    OMIM # 607616
    Niemann-Pick Disease, Type E, Niemann-Pick Disease, Type F, Niemann-Pick Disease, Intermediate, with Visceral Involvement and Rapid Progression,
  • Sphingomyelin Phosphodiesterase 1, Acid Lysosomal
    OMIM # 607608
    SMPD1, Sphingomyelinase, Acid, ASM
  • Ichthyosis, Spastic Quadriplegia, and Mental Retardation
    OMIM # 614457
    ISQMR
  • ELOVL4 Gene
    OMIM # 605512
    Elongation of Very Long Chain Fatty Acids-Like 4, ELOVL4
  • Retinitis Pigmentosa 12
    OMIM # 600105
    RP12, Retinitis Pigmentosa with or without Paraarteriolar Preservation of Retinal Pigment Epithelium, RP with or without Preserved Paraarteriole Retinal Pigment Epithelium, RP with or without PPRPE,
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