Stromová štruktúra MeSH - choroby z deficitu manozidázy

[c16.320.565.202.607]

• 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]
          • alfa-manozidóza [c16.320.565.202.607.500]
          • beta-manozidóza [c16.320.565.202.607.750]
        • 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] +

[c16.320.565.595.577]

• 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] +
        • aspartylglukozaminúria [c16.320.565.595.100]
        • choroba z ukladania esterov cholesterolu [c16.320.565.595.201] +
        • cystinóza [c16.320.565.595.377]
        • choroby lyzozómové, nervového systému [c16.320.565.595.554] +
        • choroby z deficitu manozidázy [c16.320.565.595.577]
          • alfa-manozidóza [c16.320.565.595.577.500]
          • beta-manozidóza [c16.320.565.595.577.750]
        • mukopolysacharidózy [c16.320.565.595.600] +
        • pyknodysostóza [c16.320.565.595.800]

[c18.452.648.202.607]

• 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]
          • alfa-manozidóza [c18.452.648.202.607.500]
          • beta-manozidóza [c18.452.648.202.607.750]
        • 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] +

[c18.452.648.595.577]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • poruchy metabolizmu, vrodené [c18.452.648] +
      • choroby lyzozómové [c18.452.648.595] +
        • aspartylglukozaminúria [c18.452.648.595.100]
        • choroba z ukladania esterov cholesterolu [c18.452.648.595.201] +
        • cystinóza [c18.452.648.595.377]
        • choroby lyzozómové, nervového systému [c18.452.648.595.554] +
        • choroby z deficitu manozidázy [c18.452.648.595.577]
          • alfa-manozidóza [c18.452.648.595.577.500]
          • beta-manozidóza [c18.452.648.595.577.750]
        • mukopolysacharidózy [c18.452.648.595.600] +
        • pyknodysostóza [c18.452.648.595.800]