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CTGA Database Listing
Arab Genomic Studies
Records found: 2572 Sort by:
  • Tumor Protein p63
    OMIM # 603273
    TP63, Tumor Protein p73-Like, TP73L, p53-Related Protein p63, p63, KET
  • Desmoplakin
    OMIM # 125647
    DSP, Desmoplakin I, DSPI, Desmoplakin II, DSPII
  • Cockayne Syndrome B
    OMIM # 133540
    CSB, Cockayne Syndrome Type II,
  • Excision Repair Cross-Complementing, Group 6
    OMIM # 609413
    ERCC6, RAD26, S. Cerevisiae, Homolog of , CSB Gene
  • 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
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