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CTGA Database Listing
Arab Genomic Studies
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  • Cornelia de Lange Syndrome 1
    OMIM # 122470
    CDLS1, CDL, CDLS, Typus Degenerativus Amstelodamensis, De Lange Syndrome, Brachmann-de Lange Syndrome, BDLS
  • Schnyder Corneal Dystrophy
    OMIM # 121800
    SCCD, Crystalline Stromal Dystrophy, Hereditary Crystalline Stromal Dystrophy of Schnyder, SCD, Schnyder Crystalline Corneal Dystrophy, Schnyder Crystalline Dystrophy Sine Crystals,
  • Febrile Convulsions, Familial, 1
    OMIM # 121210
    FEB1, Convulsions, Familial Febrile, 1
  • Seizures, Benign Familial Neonatal, 1
    OMIM # 121200
    BFNS1, Epilepsy, Benign Neonatal, 1, and/or Myokymia, Included, Seizures, Benign Familial Neonatal, 1, and/or Myokymia
  • Arthrogryposis, Distal, Type 9
    OMIM # 121050
    DA9, Contractural Arachnodactyly, Congenital, CCA, Beals Syndrome
  • Lynch Syndrome I
    OMIM # 120435
    Colorectal Cancer, Hereditary Nonpolyposis, Type 1, HNPCC1, Colon Cancer, Familial Nonpolyposis, Type 1, FCC1, COCA1, Lynch Syndrome II
  • 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
  • Papillorenal Syndrome
    OMIM # 120330
    Renal-Coloboma Syndrome, Optic Nerve Coloboma with Renal Disease, Coloboma of Optic Nerve with Renal Disease, Optic Coloboma, Vesicoureteral Reflux, and Renal Anomalies, Renal-Coloboma Syndrome with Macular Abnormalities, Renal Hypoplasia, Isolated
  • Coarctation of Aorta
    OMIM # 120000
  • Cluster Headache, Familial
    OMIM # 119915
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