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CTGA Database Listing
Arab Genomic Studies
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  • Vitamin D-Dependent Rickets, Type II
    OMIM # 277440
    VDDR2A, Vitamin D-Dependent Rickets, Type 2a, with or without Alopecia, Rickets, Hereditary Vitamin D-Resistant, HVDRR, Generalized Resistance to 1,25-Dihydroxyvitamin D, Vitamin D-Resistant Rickets with End-Organ Unresponsiveness to 1,25-Dihydroxycholecalciferol, Pseudovitamin D-Deficiency, Type IIA, PDDR IIA, Hypocalcemic Vitamin D-Resistant Rickets, HVDRR, Rickets-Alopecia Syndrome
  • Vitamin A Metabolic Defect (*)
    OMIM # 277350
  • Visceral Myopathy, Familial, with External Ophthalmoplegia (*)
    OMIM # 277320
    Intestinal Pseudoobstruction with External Ophthalmoplegia, Muscular Dystrophy, Oculogastrointestinal,
  • Vici Syndrome (*)
    OMIM # 242840
    VICIS, Immunodeficiency with Cleft Lip/Palate, Cataract, Hypopigmenation, and Absent Corpus Callosum
  • Vesicoureteral Reflux 1
    OMIM # 193000
    CAKUT, Congenital Anomalies of Kidney and Urinary Tract, VUR, VUR1
  • Vas Deferens, Congenital Bilateral Aplasia of
    OMIM # 277180
    CBAVD, CAVD
  • Van der Woude Syndrome
    OMIM # 119300
    VWS, VDWS, Lip-Pit Syndrome , LPS, PIT, Cleft Lip and/or Palate with Mucous Cysts of Lower Lip,
  • Usher Syndrome, Type III (*)
    OMIM # 276902
    USH3
  • Usher Syndrome, Type IIA (*)
    OMIM # 276901
    USH2A
  • Usher Syndrome, Type IG (*)
    OMIM # 606943
    USH1G
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