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CTGA Database Listing
Arab Genomic Studies
Records found: 2274 Sort by:
  • Deafness, Autosomal Recessive 84
    OMIM # 613391
    DFNB84, Deafness, Autosomal Recessive 84, with Vestibular Dysfunction
  • Protein-Tyrosine Phosphatase, Receptor-Type, Q
    OMIM # 603317
    PTPRQ, Protein-tyrosine Phosphatase, Receptor-Type, Expressed by Glomerular Mesangial Cells 1, PTPGMC1
  • Alzheimer Disease
    OMIM # 104300
    AD, Presenile and Senile Dementia, Alzheimer Disease, Familial, 1, Included, AD1, Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy, Included, Alzheimer Disease, Protection Against
  • 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
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