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CTGA Database Listing
Arab Genomic Studies
Records found: 2565 Sort by:
  • Teeth, Supernumerary
    OMIM # 187100
    Hyperdontia
  • Synpolydactyly 1
    OMIM # 186000
    SPD1, Synpolydactyly, Type II, SDTY2
  • Chromosome 2q35 Duplication Syndrome
    OMIM # 185900
    Syndactyly, Type I, SDTY1, SD1, Zygodactyly
  • 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
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