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Displaying 20 of 209,107 results for " "
  1. NM_171998.3(RAB39B):c.215+1G>A AND Mental retardation, X-linked 72

    Type: Variation

    Species: human

  2. GPR143, 19-BP DUP AND Nystagmus 6, congenital, X-linked

    Type: Variation

    Species: human

  3. F9, EX7DEL AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  4. NM_000133.3(F9):c.655C>T (p.Gln219Ter) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  5. NM_000133.3(F9):c.804T>G (p.Cys268Trp) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  6. NM_000133.3(F9):c.82T>C (p.Cys28Arg) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  7. NM_000133.3(F9):c.237A>C (p.Glu79Asp) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  8. F9, EX1-3DEL AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  9. NM_000133.3(F9):c.1150C>T (p.Arg384Ter) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  10. NM_000133.3(F9):c.1070G>A (p.Gly357Glu) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  11. NM_000133.3(F9):c.329A>G (p.Asp110Gly) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  12. NM_000133.3(F9):c.709C>T (p.Gln237Ter) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  13. NM_000133.3(F9):c.52T>C (p.Cys18Arg) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  14. NM_000133.3(F9):c.1144T>C (p.Cys382Arg) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  15. NM_000133.3(F9):c.31T>A (p.Ser11Thr) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  16. F9, EX1-8DEL AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  17. NM_000133.3(F9):c.479G>C (p.Gly160Ala) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  18. F9, 1-BP DEL, +13A AND Hemophilia B Leyden

    Type: Variation

    Species: human

  19. NM_000133.3(F9):c.1307C>T (p.Ala436Val) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human

  20. NM_000133.3(F9):c.316G>A (p.Gly106Ser) AND Hereditary factor IX deficiency disease

    Type: Variation

    Species: human


Displaying 20 of 209,107 results for " "