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CTGA Database Listing
Arab Genomic Studies
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  • Mental Retardation, X-Linked 30(*)
    OMIM # 300558
    MRX30, Mental Retardation, X-Linked 47, MRX47
  • 3-Hydroxy-3-Methylglutaryl-CoA Lyase
    OMIM # 613898
    HMGCL, HMG-CoA Lyase, HL
  • Titin (*)
    OMIM # 188840
    TTN, Connectin
  • Coronary Artery Disease, Autosomal Dominant, 1
    OMIM # 608320
    ADCAD1
  • Hemophagocytic Lymphohistiocytosis, Familial, 2
    OMIM # 603553
    FHL2, HPLH2, HLH2
  • Knobloch Syndrome 1
    OMIM # 267750
    KNO1, KNO, Retinal Detachment and Occipital Encephalocele
  • Hemophagocytic Lymphohistiocytosis, Familial, 1
    OMIM # 267700
    FHL1, HPLH1, HLH1, Hemophagocytic Lymphohistiocytosis, Familial, FHL, FHLH, HPLH, Reticulosis, Familial Histiocytic, Hemophagocytic Reticulosis, Familial, Erythrophagocytic Lymphohistiocytosis, Familial, FEL
  • Geroderma Osteodysplasticum
    OMIM # 231070
    GO, Gerodermia Osteodysplastica, Osteoplastic Geroderma Walt Disney Dwarfism, Premature Senility Syndrome, Bamatter's syndrome, Bamatter-Franceschetti-Klein-Sierro Syndrome, Walt Disney Dwarfism,
  • Perforin 1
    OMIM # 170280
    PRF1, PFN1, Pore-Forming Protein, PFP
  • Collagen, Type XVIII, Alpha-1
    OMIM # 120328
    COL18A1, Endostatin
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