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CTGA Database Listing
Arab Genomic Studies
Records found: 2588 Sort by:
  • Weaver Syndrome
    OMIM # 277590
    Weaver-Smith Syndrome, WSS, Weaver-like Syndrome
  • Weill-Marchesani Syndrome, Autosomal Recessive
    OMIM # 277600
    WM Syndrome, WMS, Spherophakia-Brachymorphia Syndrome, Mesodermal Dysmorphodystrophy, Congenital,
  • Werner Syndrome
    OMIM # 277700
    WRN
  • Lysosomal Acid Lipase Deficiency
    OMIM # 278000
    Cholesteryl Ester Storage Disease, CESD, LIPA Deficiency, LAL Deficiency Cholesterol Ester Hydrolase Deficiency, Wolman Disease
  • Wrinkly Skin Syndrome
    OMIM # 278250
    WSS
  • Xeroderma Pigmentosum, Complementation Group A
    OMIM # 278700
    XPA, XP Group A, Xeroderma Pigmentosum I, XP1
  • Xeroderma Pigmentosum, Complementation Group C
    OMIM # 278720
    XPC, XPCC, XP, Group C, Xeroderma Pigmentosum III, XP3, XPC Gene,
  • Young Syndrome
    OMIM # 279000
    Azoospermia, Obstructive, and Chronic Sinopulmonary Infections, Sinusitis-Infertility Syndrome, Barry-Perkins-Young Syndrome,
  • Opitz GBBB Syndrome, X-Linked
    OMIM # 300000
    Opitz GBBB Syndrome, Type I, GGGB1, Opitz Syndrome, OS, Opitz Syndrome, X-Linked, OSX, Opitz-G Syndrome, Type I, OGS1, Opitz BBBG Syndrome, Type I, BBBG1, Hypertelorism with Esophageal Abnormality and Hypospadias, Hypertelorism-Hypospadias Syndrome, Telecanthus-Hypospadias Syndrome
  • Microphthalmia with Limb Anomalies
    OMIM # 206920
    MLA, Anophthalmia with Limb Anomalies, Waardenburg Anophthalmia Syndrome, Anophthalmia-Syndactyly, Ophthalmoacromelic Syndrome, Waardenburg Recessive Anophthalmia Syndrome, Anophthalmia-Waardenburg Syndrome, Anophthalmos-Limb Anomalies Syndrome, Crooked Fingers Syndrome, Syndactyly-Anophthalmos Syndrome
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