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CTGA Database Listing
Arab Genomic Studies
Records found: 2572 Sort by:
  • Sturge-Weber Syndrome
    OMIM # 185300
    SWS
  • Strabismus, Susceptibility to
    OMIM # 185100
    Strabismus, Susceptibility to, 1, STBMS1
  • Polycystic Ovary Syndrome 1
    OMIM # 184700
    PCOS1, PCO1, PCO, PCOS, Stein-Leventhal Syndrome, Hyperandrogenemia
  • Spondyloepimetaphyseal Dysplasia, Maroteaux Type
    OMIM # 184095
    Brachyolmia, Maroteaux Type, SED, Maroteaux Type, Pseudo-Morquio Syndrome, Type 2
  • Neural Tube Defects, Susceptibility to
    OMIM # 182940
    NTD, Spina Bifida
  • Spherocytosis, Type I
    OMIM # 182900
    Spherocytosis, Hereditary, 1, HS1, SPH, HS
  • Nail Disorder, Nonsyndromic Congenital, 4
    OMIM # 206800
    NDNC4, Anonychia/Hyponychia Congenita, Anonychia Totalis
  • R-Spondin Family, Member 4
    OMIM # 610573
    RSPO4 , CRISTIN4
  • Vitamin D Receptor
    OMIM # 601769
    VDR, 1,25-Dihydroxyvitamin D3 Receptor, Vitamin D Hormone Receptor,
  • Spastic Paraplegia 3, Autosomal Dominant
    OMIM # 182600
    SPG3A, SPG3, Strumpell Disease, Familial Spastic Paraplegia, Autosomal Dominant, 1, FSP1
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