Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2571 Sort by:
  • Wingless-Type MMTV Integration Site Family, Member 10A
    OMIM # 606268
    WNT10A
  • Tumoral Calcinosis, Hyperphosphatemic, Familial, 2
    OMIM # 617993
    HFTC2 , Hyperphosphatemic Hyperostosis Syndrome
  • Fibroblast Growth Factor 23
    OMIM # 605380
    FGF23
  • Odontoonychodermal Dysplasia
    OMIM # 257980
    OODD, Fadhil Syndrome
  • Hypomagnesemia 3, Renal
    OMIM # 248250
    HOMG3, FHHNC, Familial Hypercalciuric Hypomagnesemia, and Nephrocalcinosis, Hypomagnesemia, Primary Magnesium, Defect in Renal Tubular Transport of, Hypomagnesemia, Primary, due to Defect in Renal Tubular Transport of Magnesium, Hypomagnesemia, Isolated Renal, Hypomagnesemia, Familial, with Hypercalciuria and Nephrocalcinosis
  • Claudin 16
    OMIM # 603959
    CLDN16 , Paracellin 1 , PCLN1
  • Achromatopsia 2
    OMIM # 216900
    ACHM2, Colorblindness, Total, Rod Monochromatism 2, Rod Monochromacy 2, RMCH2,
  • Citrullinemia, Classic
    OMIM # 215700
    Citrullinemia, Type I, CTLN1, Citrullinuria, Argininosuccinate Synthetase Deficiency, ASS Deficiency
  • Chorioretinal Dystrophy, Spinocerebellar Ataxia, and Hypogonadotropic Hypogonadism
    OMIM # 215470
    Boucher-Neuhauser Syndrome
  • Rhizomelic Chondrodysplasia Punctata, Type 1
    OMIM # 215100
    RCDP1, Chondrodysplasia Punctata, Rhizomelic Form, CDPR, Chondrodystrophia Calcificans Punctata, PTS2 Deficiency, Alkylglycerone Phosphate Synthase Deficiency,
  1. <<
  2. 1
  3. 2
  4. 3
  5. 4
  6. 5
  7. 6
  8. 7
  9. 8
  10. 9
  11. 10
  12. 11
  13. 12
  14. 13
  15. ...
  16. >>