Stromová štruktúra MeSH - hypofosfatázia

[c16.320.565.618.482]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • poruchy metabolizmu, vrodené [c16.320.565] +
      • poruchy metabolizmu kovov, vrodené [c16.320.565.618] +
        • hemochromatóza [c16.320.565.618.337]
        • degenerácia hepatolentikulárna [c16.320.565.618.403]
        • hypofosfatázia [c16.320.565.618.482]
        • hypofosfatémia familiárna [c16.320.565.618.544] +
        • Menkesov syndróm [c16.320.565.618.590]
        • paralýzy familiárne periodické [c16.320.565.618.711] +
        • pseudohypoparatyreóza [c16.320.565.618.815] +

[c18.452.648.618.482]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • poruchy metabolizmu, vrodené [c18.452.648] +
      • poruchy metabolizmu kovov, vrodené [c18.452.648.618] +
        • hemochromatóza [c18.452.648.618.337]
        • degenerácia hepatolentikulárna [c18.452.648.618.403]
        • hypofosfatázia [c18.452.648.618.482]
        • hypofosfatémia familiárna [c18.452.648.618.544] +
        • Menkesov syndróm [c18.452.648.618.590]
        • paralýzy familiárne periodické [c18.452.648.618.711] +
        • pseudohypoparatyreóza [c18.452.648.618.815] +