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CTGA Database Listing
Arab Genomic Studies
Records found: 2567 Sort by:
  • Odontoonychodermal Dysplasia
    OMIM # 257980
    OODD, Fadhil Syndrome
  • Wingless-Type MMTV Integration Site Family, Member 10A
    OMIM # 606268
    WNT10A
  • Hypomagnesemia 3, Renal
    OMIM # 248250
    HOMG3, FHHNC, Familial Hypercalciuric Hypomagnesemia, and Nephrocalcinosis, Hypomagnesemia, Primary Magnesium, Defect in Renal Tubular Transport of, Hypomagnesemia, Primary, due to Defect in Renal Tubular Transport of Magnesium, Hypomagnesemia, Isolated Renal, Hypomagnesemia, Familial, with Hypercalciuria and Nephrocalcinosis
  • Claudin 16
    OMIM # 603959
    CLDN16 , Paracellin 1 , PCLN1
  • Achromatopsia 2
    OMIM # 216900
    ACHM2, Colorblindness, Total, Rod Monochromatism 2, Rod Monochromacy 2, RMCH2,
  • Citrullinemia, Classic
    OMIM # 215700
    Citrullinemia, Type I, CTLN1, Citrullinuria, Argininosuccinate Synthetase Deficiency, ASS Deficiency
  • Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
    OMIM # 215470
    Boucher-Neuhauser Syndrome
  • Rhizomelic Chondrodysplasia Punctata, Type 1
    OMIM # 215100
    RCDP1, Chondrodysplasia Punctata, Rhizomelic Form, CDPR, Chondrodystrophia Calcificans Punctata, PTS2 Deficiency, Alkylglycerone Phosphate Synthase Deficiency,
  • Cholestasis-Lymphedema Syndrome
    OMIM # 214900
    CHLS, Aagenaes Syndrome, Lymphedema-Cholestasis Syndrome, LCS, LCS1
  • CHARGE Syndrome
    OMIM # 214800
    Charge Association--Coloboma, Heart Anomaly, Choanal Atresia, Retardation, Genital and Ear Anomalies, Hall-Hittner Syndrome, HHS
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