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CTGA Database Listing
Arab Genomic Studies
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  • Aarskog-Scott Syndrome
    OMIM # 305400
    AAS, Faciogenital Dysplasia, FGDY, Faciodigitogenital Syndrome, Aarskog Syndrome, X-Linked, Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder, Mental Retardation, X-Linked, Syndromic 16, MRXS16,
  • Dyskeratosis Congenita, X-linked
    OMIM # 305000
    DKC, Zinsser-Cole-Engman Syndrome, DKCX
  • Diabetes Insipidus, Nephrogenic, X-Linked
    OMIM # 304800
    NDI, Diabetes Insipidus, Nephrogenic, Type I
  • Corpus Callosum, Partial Agenesis of, X-Linked
    OMIM # 304100
  • Aicardi Syndrome
    OMIM # 304050
    AIC, Corpus Callosum, Agenesis of, with Chorioretinal Abnormality
  • Colorblindness, Partial, Protan Series
    OMIM # 303900
    CBP, Protanopia, Red Colorblindness,
  • Colorblindness, Partial, Deutan Series
    OMIM # 303800
    CBD, Deutan Colorblindness, DCB, Deuteranopia, Green Colorblindness,
  • Coffin-Lowry Syndrome
    OMIM # 303600
    CLS
  • MASA Syndrome
    OMIM # 303350
    Mental Retardation, Aphasia, Shuffling Gait, and Adducted Thumbs, Clasped Thumb and Mental Retardation, Thumb, Congenital Clasped, with Mental Retardation, Adducted Thumb with Mental Retardation, Gareis-Mason Syndrome, Spastic Paraplegia Type 1, SPG1, Crash Syndrome,
  • Chondrodysplasia Punctata 2, X-Linked Dominant
    OMIM # 302960
    CDPX2, CDPXD, CPXD, Conradi-Hunermann Syndrome, Happle Syndrome, Conradi-Hunermann-Happle Syndrome,
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