MeSH Tree Structures - mukolipidózy

[c05.116.198.371]

• choroby muskuloskeletárne [c05] +
  • choroby kostí [c05.116] +
    • choroby kostí, metabolické [c05.116.198] +
      • demineralizácia kostí, patologická [c05.116.198.247] +
      • mukolipidózy [c05.116.198.371]
      • osteoporóza [c05.116.198.579] +
      • pseudohypoparatyreóza [c05.116.198.709] +
      • rachitída [c05.116.198.816] +

[c10.228.140.163.100.435.590]

• 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] +
          • choroby lyzozómové, nervového systému [c10.228.140.163.100.435] +
            • fukozidóza [c10.228.140.163.100.435.295]
            • glykogenóza, typ II [c10.228.140.163.100.435.340]
            • mukolipidózy [c10.228.140.163.100.435.590]
            • choroba z ukladania kyseliny sialovej [c10.228.140.163.100.435.810]
            • sfingolipidózy [c10.228.140.163.100.435.825] +

[c16.320.565.189.435.590]

• 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] +
        • choroby lyzozómové, nervového systému [c16.320.565.189.435] +
          • fukozidóza [c16.320.565.189.435.295]
          • glykogenóza, typ II [c16.320.565.189.435.340]
          • mukolipidózy [c16.320.565.189.435.590]
          • choroba z ukladania kyseliny sialovej [c16.320.565.189.435.810]
          • sfingolipidózy [c16.320.565.189.435.825] +

[c16.320.565.202.670]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • poruchy metabolizmu, vrodené [c16.320.565] +
      • poruchy metabolizmu sacharidov, vrodené [c16.320.565.202] +
        • poruchy glykozylácie, vrodené [c16.320.565.202.125]
        • poruchy metabolizmu fruktózy, vrodené [c16.320.565.202.251] +
        • fukozidóza [c16.320.565.202.303]
        • galaktozémie [c16.320.565.202.355]
        • deficit glukózafosfátdehydrogenázy [c16.320.565.202.402]
        • glykogenóza [c16.320.565.202.449] +
        • hyperoxalúria primárna [c16.320.565.202.460]
        • intolerancia laktózy [c16.320.565.202.589]
        • choroby z deficitu manozidázy [c16.320.565.202.607] +
        • mukolipidózy [c16.320.565.202.670]
        • mukopolysacharidózy [c16.320.565.202.715] +
        • deficit karboxylázy, mnohopočetný [c16.320.565.202.720] +
        • poruchy metabolizmu pyruvátu, vrodené [c16.320.565.202.810] +

[c16.320.565.595.554.590]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • poruchy metabolizmu, vrodené [c16.320.565] +
      • choroby lyzozómové [c16.320.565.595] +
        • choroby lyzozómové, nervového systému [c16.320.565.595.554] +
          • fukozidóza [c16.320.565.595.554.295]
          • glykogenóza, typ II [c16.320.565.595.554.340]
          • mukolipidózy [c16.320.565.595.554.590]
          • choroba z ukladania kyseliny sialovej [c16.320.565.595.554.810]
          • sfingolipidózy [c16.320.565.595.554.825] +

[c18.452.132.100.435.590]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • choroby mozgu, metabolické [c18.452.132] +
      • choroby mozgu, metabolické vrodené [c18.452.132.100] +
        • choroby lyzozómové, nervového systému [c18.452.132.100.435] +
          • fukozidóza [c18.452.132.100.435.295]
          • glykogenóza, typ II [c18.452.132.100.435.340]
          • mukolipidózy [c18.452.132.100.435.590]
          • choroba z ukladania kyseliny sialovej [c18.452.132.100.435.810]
          • sfingolipidózy [c18.452.132.100.435.825] +

[c18.452.648.189.435.590]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • poruchy metabolizmu, vrodené [c18.452.648] +
      • choroby mozgu, metabolické vrodené [c18.452.648.189] +
        • choroby lyzozómové, nervového systému [c18.452.648.189.435] +
          • fukozidóza [c18.452.648.189.435.295]
          • glykogenóza, typ II [c18.452.648.189.435.340]
          • mukolipidózy [c18.452.648.189.435.590]
          • choroba z ukladania kyseliny sialovej [c18.452.648.189.435.810]
          • sfingolipidózy [c18.452.648.189.435.825] +

[c18.452.648.202.670]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • poruchy metabolizmu, vrodené [c18.452.648] +
      • poruchy metabolizmu sacharidov, vrodené [c18.452.648.202] +
        • poruchy glykozylácie, vrodené [c18.452.648.202.125]
        • poruchy metabolizmu fruktózy, vrodené [c18.452.648.202.251] +
        • fukozidóza [c18.452.648.202.303]
        • galaktozémie [c18.452.648.202.355]
        • deficit glukózafosfátdehydrogenázy [c18.452.648.202.402]
        • glykogenóza [c18.452.648.202.449] +
        • hyperoxalúria primárna [c18.452.648.202.460]
        • intolerancia laktózy [c18.452.648.202.589]
        • choroby z deficitu manozidázy [c18.452.648.202.607] +
        • mukolipidózy [c18.452.648.202.670]
        • mukopolysacharidózy [c18.452.648.202.715] +
        • deficit karboxylázy, mnohopočetný [c18.452.648.202.720] +
        • poruchy metabolizmu pyruvátu, vrodené [c18.452.648.202.810] +

[c18.452.648.595.554.590]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • poruchy metabolizmu, vrodené [c18.452.648] +
      • choroby lyzozómové [c18.452.648.595] +
        • choroby lyzozómové, nervového systému [c18.452.648.595.554] +
          • fukozidóza [c18.452.648.595.554.295]
          • glykogenóza, typ II [c18.452.648.595.554.340]
          • mukolipidózy [c18.452.648.595.554.590]
          • choroba z ukladania kyseliny sialovej [c18.452.648.595.554.810]
          • sfingolipidózy [c18.452.648.595.554.825] +

MeSH Tree Structures - hexozaminidázy

[d08.811.277.450.483]

• enzýmy a koenzýmy [d08] +
  • enzýmy [d08.811] +
    • hydrolázy [d08.811.277] +
      • glykozidhydrolázy [d08.811.277.450] +
        • alfa-L-fukozidáza [d08.811.277.450.050]
        • amylázy [d08.811.277.450.066] +
        • beta-fruktofuranozidáza [d08.811.277.450.114]
        • chitinázy [d08.811.277.450.207] +
        • dextranáza [d08.811.277.450.283]
        • disacharidázy [d08.811.277.450.329] +
        • galaktozidázy [d08.811.277.450.410] +
        • glukozidázy [d08.811.277.450.420] +
        • glukuronidáza [d08.811.277.450.426] +
        • N-glykozyl hydrolázy [d08.811.277.450.430] +
        • hexozaminidázy [d08.811.277.450.483]
          • alfa-N-acetylgalaktozaminidáza [d08.811.277.450.483.044]
          • beta-N-acetylgalaktozaminidáza [d08.811.277.450.483.112]
          • beta-N-acetylhexozaminidázy [d08.811.277.450.483.180] +
          • manozyl-glykoproteín-endo-beta-N-acetylglukozaminidáza [d08.811.277.450.483.765]
        • hyalurónglukózaminidáza [d08.811.277.450.529]
        • iduronidáza [d08.811.277.450.560]
        • izoamyláza [d08.811.277.450.585]
        • manozidázy [d08.811.277.450.625] +
        • muramidáza [d08.811.277.450.642]
        • neuraminidáza [d08.811.277.450.692]
        • oligo-1,6-glukozidáza [d08.811.277.450.770] +
        • polygalakturonáza [d08.811.277.450.800]
        • xylozidázy [d08.811.277.450.950] +