MeSH Tree Structures - deficit acyl-CoA dehydrogenázy, mnohopočetný

[c16.320.565.100.614]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • poruchy metabolizmu, vrodené [c16.320.565] +
      • poruchy metabolizmu aminokyselín, vrodené [c16.320.565.100] +
        • albinizmus [c16.320.565.100.102] +
        • alkaptonúria [c16.320.565.100.187]
        • hyperglycinémia neketotická [c16.320.565.100.477]
        • hyperhomocysteinémia [c16.320.565.100.480] +
        • hyperlyzinémie [c16.320.565.100.544]
        • leucinóza [c16.320.565.100.608]
        • deficit acyl-CoA dehydrogenázy, mnohopočetný [c16.320.565.100.614]
        • deficit karboxylázy, mnohopočetný [c16.320.565.100.620] +
        • fenylketonúrie [c16.320.565.100.766] +
        • deficit prolidázy [c16.320.565.100.794]
        • acidémia propiónová [c16.320.565.100.823]
        • tyrozinémie [c16.320.565.100.880]
        • poruchy močovinového cyklu, vrodené [c16.320.565.100.940] +

[c18.452.648.100.614]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • poruchy metabolizmu, vrodené [c18.452.648] +
      • poruchy metabolizmu aminokyselín, vrodené [c18.452.648.100] +
        • albinizmus [c18.452.648.100.102] +
        • alkaptonúria [c18.452.648.100.187]
        • hyperglycinémia neketotická [c18.452.648.100.477]
        • hyperhomocysteinémia [c18.452.648.100.480] +
        • hyperlyzinémie [c18.452.648.100.544]
        • leucinóza [c18.452.648.100.608]
        • deficit acyl-CoA dehydrogenázy, mnohopočetný [c18.452.648.100.614]
        • deficit karboxylázy, mnohopočetný [c18.452.648.100.620] +
        • fenylketonúrie [c18.452.648.100.766] +
        • acidémia propiónová [c18.452.648.100.823]
        • tyrozinémie [c18.452.648.100.880]
        • poruchy močovinového cyklu, vrodené [c18.452.648.100.940] +

[c18.452.660.612]

• choroby metabolické a poruchy výživy [c18] +
  • choroby metabolické [c18.452] +
    • mitochondriopatie [c18.452.660] +
      • choroba z deficitu karbamoylfosfát syntázy I [c18.452.660.097]
      • deficit cytochróm-c oxidázy [c18.452.660.195]
      • Friedreichova ataxia [c18.452.660.300]
      • Leighov syndróm [c18.452.660.520]
      • myopatie mitochondriálne [c18.452.660.560] +
      • deficit acyl-CoA dehydrogenázy, mnohopočetný [c18.452.660.612]
      • atrofia zrakového nervu, autozomálne dominantná [c18.452.660.665]
      • Leberova hereditárna optická neuropatia [c18.452.660.670]
      • choroba z deficitu pyruvátkarboxylázy [c18.452.660.705]
      • choroba z deficitu pyruvátdehydrogenázového komplexu [c18.452.660.710]