Stromová štruktúra MeSH - Hartnupova choroba

[c10.228.140.163.100.355]

• choroby nervového systému [c10] +
  • choroby centrálneho nervového systému [c10.228] +
    • choroby mozgu [c10.228.140] +
      • choroby mozgu, metabolické [c10.228.140.163] +
        • choroby mozgu, metabolické vrodené [c10.228.140.163.100] +
          • adrenoleukodystrofia [c10.228.140.163.100.084]
          • angiopatia cerebrálna amyloidná familiárna [c10.228.140.163.100.168]
          • galaktozémie [c10.228.140.163.100.320]
          • Hartnupova choroba [c10.228.140.163.100.355]
          • degenerácia hepatolentikulárna [c10.228.140.163.100.360]
          • choroby centrálneho nervového systému demyelinizačné, dedičné [c10.228.140.163.100.362] +
          • homocystinúria [c10.228.140.163.100.365]
          • hyperglycinémia neketotická [c10.228.140.163.100.375]
          • hyperlyzinémie [c10.228.140.163.100.380]
          • Leighov syndróm [c10.228.140.163.100.412]
          • Leschov-Nyhanov syndróm [c10.228.140.163.100.425]
          • choroby lyzozómové, nervového systému [c10.228.140.163.100.435] +
          • leucinóza [c10.228.140.163.100.520]
          • MELAS syndróm [c10.228.140.163.100.535]
          • Menkesov syndróm [c10.228.140.163.100.540]
          • MERRF syndróm [c10.228.140.163.100.545]
          • deficit mevalonátkinázy [c10.228.140.163.100.593]
          • syndróm okulocerebrorenálny [c10.228.140.163.100.640]
          • fenylketonúrie [c10.228.140.163.100.687] +
          • choroba z deficitu pyruvátkarboxylázy [c10.228.140.163.100.725]
          • choroba z deficitu pyruvátdehydrogenázového komplexu [c10.228.140.163.100.750]
          • Refsumova choroba [c10.228.140.163.100.813]
          • Refsumova choroba, infantilný typ [c10.228.140.163.100.844]
          • tyrozinémie [c10.228.140.163.100.875]
          • poruchy močovinového cyklu, vrodené [c10.228.140.163.100.937] +
          • Zellwegerov syndróm [c10.228.140.163.100.968]

[c12.050.351.968.419.815.885.625]

• choroby urogenitálne [c12] +
  • choroby ženské urogenitálne a komplikácie v gravidite [c12.050] +
    • choroby urogenitálne ženské [c12.050.351] +
      • choroby urologické [c12.050.351.968] +
        • choroby obličiek [c12.050.351.968.419] +
          • poruchy renálneho tubulárneho transportu, vrodené [c12.050.351.968.419.815] +
            • aminoacidúrie renálne [c12.050.351.968.419.815.885] +
              • cystinúria [c12.050.351.968.419.815.885.250]
              • Hartnupova choroba [c12.050.351.968.419.815.885.625]

[c12.200.777.419.815.885.457]

• choroby urogenitálne [c12] +
  • choroby urogenitálne mužské [c12.200] +
    • choroby urologické [c12.200.777] +
      • choroby obličiek [c12.200.777.419] +
        • poruchy renálneho tubulárneho transportu, vrodené [c12.200.777.419.815] +
          • aminoacidúrie renálne [c12.200.777.419.815.885] +
            • cystinúria [c12.200.777.419.815.885.250]
            • Hartnupova choroba [c12.200.777.419.815.885.457]

[c12.950.419.815.885.625]

• choroby urogenitálne [c12] +
  • choroby urologické [c12.950] +
    • choroby obličiek [c12.950.419] +
      • poruchy renálneho tubulárneho transportu, vrodené [c12.950.419.815] +
        • aminoacidúrie renálne [c12.950.419.815.885] +
          • cystinúria [c12.950.419.815.885.250]
          • Hartnupova choroba [c12.950.419.815.885.625]

[c16.320.565.151.355]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • poruchy metabolizmu, vrodené [c16.320.565] +
      • poruchy transportu aminokyselín, vrodené [c16.320.565.151] +
        • Hartnupova choroba [c16.320.565.151.355]
        • syndróm okulocerebrorenálny [c16.320.565.151.600]

[c16.320.565.189.355]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • poruchy metabolizmu, vrodené [c16.320.565] +
      • choroby mozgu, metabolické vrodené [c16.320.565.189] +
        • adrenoleukodystrofia [c16.320.565.189.084]
        • angiopatia cerebrálna amyloidná familiárna [c16.320.565.189.168]
        • galaktozémie [c16.320.565.189.320]
        • Hartnupova choroba [c16.320.565.189.355]
        • degenerácia hepatolentikulárna [c16.320.565.189.360]
        • choroby centrálneho nervového systému demyelinizačné, dedičné [c16.320.565.189.362] +
        • homocystinúria [c16.320.565.189.365]
        • hyperglycinémia neketotická [c16.320.565.189.375]
        • hyperlyzinémie [c16.320.565.189.380]
        • Leighov syndróm [c16.320.565.189.412]
        • Leschov-Nyhanov syndróm [c16.320.565.189.425]
        • choroby lyzozómové, nervového systému [c16.320.565.189.435] +
        • leucinóza [c16.320.565.189.520]
        • MELAS syndróm [c16.320.565.189.535]
        • Menkesov syndróm [c16.320.565.189.540]
        • MERRF syndróm [c16.320.565.189.545]
        • deficit mevalonátkinázy [c16.320.565.189.593]
        • syndróm okulocerebrorenálny [c16.320.565.189.640]
        • fenylketonúrie [c16.320.565.189.687] +
        • choroba z deficitu pyruvátkarboxylázy [c16.320.565.189.725]
        • choroba z deficitu pyruvátdehydrogenázového komplexu [c16.320.565.189.750]
        • Refsumova choroba [c16.320.565.189.813]
        • Refsumova choroba, infantilný typ [c16.320.565.189.844]
        • tyrozinémie [c16.320.565.189.875]
        • poruchy močovinového cyklu, vrodené [c16.320.565.189.937] +
        • Zellwegerov syndróm [c16.320.565.189.968]

[c16.320.831.885.457]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • poruchy renálneho tubulárneho transportu, vrodené [c16.320.831] +
      • aminoacidúrie renálne [c16.320.831.885] +
        • cystinúria [c16.320.831.885.250]
        • Hartnupova choroba [c16.320.831.885.457]

[c18.452.132.100.355]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • choroby mozgu, metabolické [c18.452.132] +
      • choroby mozgu, metabolické vrodené [c18.452.132.100] +
        • adrenoleukodystrofia [c18.452.132.100.084]
        • angiopatia cerebrálna amyloidná familiárna [c18.452.132.100.168]
        • galaktozémie [c18.452.132.100.320]
        • Hartnupova choroba [c18.452.132.100.355]
        • degenerácia hepatolentikulárna [c18.452.132.100.360]
        • choroby centrálneho nervového systému demyelinizačné, dedičné [c18.452.132.100.362] +
        • homocystinúria [c18.452.132.100.365]
        • hyperglycinémia neketotická [c18.452.132.100.375]
        • hyperlyzinémie [c18.452.132.100.380]
        • Leighov syndróm [c18.452.132.100.412]
        • Leschov-Nyhanov syndróm [c18.452.132.100.425]
        • choroby lyzozómové, nervového systému [c18.452.132.100.435] +
        • leucinóza [c18.452.132.100.520]
        • MELAS syndróm [c18.452.132.100.535]
        • Menkesov syndróm [c18.452.132.100.540]
        • MERRF syndróm [c18.452.132.100.545]
        • deficit mevalonátkinázy [c18.452.132.100.593]
        • syndróm okulocerebrorenálny [c18.452.132.100.640]
        • fenylketonúrie [c18.452.132.100.687] +
        • choroba z deficitu pyruvátkarboxylázy [c18.452.132.100.725]
        • choroba z deficitu pyruvátdehydrogenázového komplexu [c18.452.132.100.750]
        • Refsumova choroba [c18.452.132.100.813]
        • Refsumova choroba, infantilný typ [c18.452.132.100.844]
        • tyrozinémie [c18.452.132.100.875]
        • poruchy močovinového cyklu, vrodené [c18.452.132.100.937] +
        • Zellwegerov syndróm [c18.452.132.100.968]

[c18.452.648.151.355]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • poruchy metabolizmu, vrodené [c18.452.648] +
      • poruchy transportu aminokyselín, vrodené [c18.452.648.151] +
        • Hartnupova choroba [c18.452.648.151.355]
        • syndróm okulocerebrorenálny [c18.452.648.151.600]

[c18.452.648.189.355]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • poruchy metabolizmu, vrodené [c18.452.648] +
      • choroby mozgu, metabolické vrodené [c18.452.648.189] +
        • adrenoleukodystrofia [c18.452.648.189.084]
        • angiopatia cerebrálna amyloidná familiárna [c18.452.648.189.168]
        • galaktozémie [c18.452.648.189.320]
        • Hartnupova choroba [c18.452.648.189.355]
        • degenerácia hepatolentikulárna [c18.452.648.189.360]
        • choroby centrálneho nervového systému demyelinizačné, dedičné [c18.452.648.189.362] +
        • homocystinúria [c18.452.648.189.365]
        • hyperglycinémia neketotická [c18.452.648.189.375]
        • hyperlyzinémie [c18.452.648.189.380]
        • Leighov syndróm [c18.452.648.189.412]
        • Leschov-Nyhanov syndróm [c18.452.648.189.425]
        • choroby lyzozómové, nervového systému [c18.452.648.189.435] +
        • leucinóza [c18.452.648.189.520]
        • MELAS syndróm [c18.452.648.189.535]
        • Menkesov syndróm [c18.452.648.189.540]
        • MERRF syndróm [c18.452.648.189.545]
        • deficit mevalonátkinázy [c18.452.648.189.593]
        • syndróm okulocerebrorenálny [c18.452.648.189.640]
        • fenylketonúrie [c18.452.648.189.687] +
        • choroba z deficitu pyruvátkarboxylázy [c18.452.648.189.725]
        • choroba z deficitu pyruvátdehydrogenázového komplexu [c18.452.648.189.750]
        • Refsumova choroba [c18.452.648.189.813]
        • Refsumova choroba, infantilný typ [c18.452.648.189.844]
        • tyrozinémie [c18.452.648.189.875]
        • poruchy močovinového cyklu, vrodené [c18.452.648.189.937] +
        • Zellwegerov syndróm [c18.452.648.189.968]