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CTGA Database Listing
Arab Genomic Studies
Records found: 2571 Sort by:
  • Wolfram Syndrome 1
    OMIM # 222300
    WFS1, WFS, Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness, DIDMOAD
  • Deafness and Myopia
    OMIM # 221200
    DFNMYP
  • Deafness, Onychodystrophy, Osteodystrophy, and Mental Retardation Syndrome
    OMIM # 220500
    DOORS, DOOR Syndrome, Digitorenocerebral Syndrome, DRC Syndrome, Brachydactyly Due to Absence Of Distal Phalanges, Eronen Syndrome
  • Split-Hand/Foot Malformation 1 with Sensorineural Hearing Loss, Autosomal Recessive
    OMIM # 220600
    SHFM1D, Deafness, Congenital, with Split Hands and Feet,
  • Dandy-Walker Syndrome
    OMIM # 220200
    DWS, Dandy-Walker Malformation , DWM
  • Cystinuria
    OMIM # 220100
    Cystinuria, Type I, Cystinuria, Type I, Formerly, CSNU1, Formerly, Cystinuria, Type II, Formerly, Cystinuria, Type III, Formerly, CSNU3, Formerly, Cystinuria, Type Non-I, Formerly, Cystinuria, Type A , Cystinuria, Type B, Cystinuria, Type A/B,
  • Cystinosis, Nephropathic
    OMIM # 219800
    CTNS, Lysosomal Cystine Transport Protein, Defect of, Cystinosin, Defect of, Cystinosis, Infantile Nephropathic , Cystinosis, Atypical Nephropathic
  • Cystic Kidney Disease with Ventriculomegaly
    OMIM # 219730
    VMCKD
  • Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Subnormal Mentality
    OMIM # 219721
  • Cystathioninuria
    OMIM # 219500
    Cystathionine Deficiency
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