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CTGA Database Listing
Arab Genomic Studies
Records found: 2565 Sort by:
  • Waardenburg Syndrome, Type 2A
    OMIM # 193510
    WS2A, Waardenburg Syndrome, Type IIA, Waardenburg Syndrome without Dystopia Canthorum, WS2
  • Von Willebrand Disease, Type 1
    OMIM # 193400
    VWD1, Von Willebrand Disease, Type I, VWD, Type 1,
  • Von Hippel-Lindau Syndrome
    OMIM # 193300
    Von Hippel-Lindau Syndrome, Modifiers of, VHL
  • Vitiligo
    OMIM # 193200
    VTLG, Halo Nevi
  • Hypophosphatemic Rickets, Autosomal Dominant
    OMIM # 193100
    ADHR, Vitamin D-Resistant Rickets, Autosomal Dominant, Hypophosphatemia, Autosomal Dominant
  • Vesicoureteral Reflux 1
    OMIM # 193000
    CAKUT, Congenital Anomalies of Kidney and Urinary Tract, VUR, VUR1
  • Tetralogy of Fallot
    OMIM # 187500
    TOF
  • GATA-Binding Protein 4
    OMIM # 600576
    GATA4
  • Transmembrane Channel-Like Protein 1
    OMIM # 606706
    TMC1, Transmembrane Cochlear-Expressed Gene 1
  • Deafness, Autosomal Recessive 7
    OMIM # 600974
    DFNB7, Deafness, Autosomal Recessive 11, DFNB11
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