Stromová štruktúra MeSH - deficit prolidázy

[c16.131.077.735]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • abnormality vrodené [c16.131] +
    • abnormality mnohopočetné [c16.131.077] +
      • syndróm delécie 22q11 [c16.131.077.019] +
      • Alagillov syndróm [c16.131.077.065]
      • Angelmanov syndróm [c16.131.077.095]
      • Barthov syndróm [c16.131.077.121]
      • syndróm bazocelulárneho névu [c16.131.077.130]
      • Beckwithov-Wiedemannov syndróm [c16.131.077.133]
      • Bloomov syndróm [c16.131.077.137]
      • syndróm branchiootorenálny [c16.131.077.208]
      • Carneyho komplex [c16.131.077.229]
      • ciliopatie [c16.131.077.245] +
      • Cockayneov syndróm [c16.131.077.250]
      • Costellov syndróm [c16.131.077.256]
      • cri-du-chat syndróm [c16.131.077.262]
      • de Langeovej syndróm [c16.131.077.272]
      • poruchy sluchu a zraku [c16.131.077.299] +
      • Donohueov syndróm [c16.131.077.313]
      • Downov syndróm [c16.131.077.327]
      • dysplázia ektodermálna [c16.131.077.350] +
      • Fraserov syndróm [c16.131.077.371]
      • Gardnerov syndróm [c16.131.077.393]
      • syndróm heterotaxie [c16.131.077.401]
      • holoprozencefália [c16.131.077.410]
      • incontinentia pigmenti [c16.131.077.445]
      • komora ľavá nekompaktná izolovaná [c16.131.077.477]
      • Laurenceov-Moonov syndróm [c16.131.077.509]
      • LEOPARD-syndróm [c16.131.077.525]
      • Loeysov-Dietzov syndróm [c16.131.077.537]
      • Marfanov syndróm [c16.131.077.550]
      • Mobiov syndróm [c16.131.077.578]
      • monilethrix [c16.131.077.592]
      • syndróm necht-jabĺčko [c16.131.077.606]
      • Nethertonov syndróm [c16.131.077.619]
      • Jadassohnov sebaceózny névus [c16.131.077.633]
      • syndróm okulocerebrorenálny [c16.131.077.662]
      • syndrómy orofaciodigitálne [c16.131.077.676]
      • Pallisterov-Hallovej syndróm [c16.131.077.690]
      • Cantrellova pentalógia [c16.131.077.696]
      • POEMS syndróm [c16.131.077.703]
      • choroby obličiek, polycystické [c16.131.077.717] +
      • Praderovej-Williho syndróm [c16.131.077.730]
      • deficit prolidázy [c16.131.077.735]
      • Proteov syndróm [c16.131.077.740]
      • syndróm prune-belly [c16.131.077.745]
      • syndróm rubeolový vrodený [c16.131.077.790]
      • Rubinsteinov-Taybiho syndróm [c16.131.077.804]
      • syndróm polydaktýlia-krátke rebrá [c16.131.077.850]
      • Silverov-Russellov syndróm [c16.131.077.855]
      • Smithov-Lemliho-Opitzov syndróm [c16.131.077.860]
      • Smithovej-Magenisovej syndróm [c16.131.077.879]
      • Sotosov syndróm [c16.131.077.889]
      • syndrómy trichotiodystrofie [c16.131.077.899]
      • syndróm trizómie 13 [c16.131.077.919]
      • syndróm trizómie 18 [c16.131.077.929]
      • Waardenburgov syndróm [c16.131.077.938]
      • Weillov-Marchesaniho syndróm [c16.131.077.941]
      • Wolfov-Hirschhornov syndróm [c16.131.077.944]
      • Zellwegerov syndróm [c16.131.077.970]

[c16.131.831.720]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • abnormality vrodené [c16.131] +
    • abnormality kožné [c16.131.831] +
      • akrodermatitída [c16.131.831.066]
      • Carneyho komplex [c16.131.831.108]
      • dyskeratóza kongenitálna [c16.131.831.150]
      • dysplázia ektodermálna [c16.131.831.350] +
      • Ehlersov-Danlosov syndróm [c16.131.831.428] +
      • epidermolysis bullosa [c16.131.831.493] +
      • ichtyóza [c16.131.831.512] +
      • incontinentia pigmenti [c16.131.831.580]
      • naevus flammeus [c16.131.831.675]
      • deficit prolidázy [c16.131.831.720]
      • pseudoxanthoma elasticum [c16.131.831.766]
      • Rothmundov-Thomsonov syndróm [c16.131.831.775]
      • scleredema neonatorum [c16.131.831.812]
      • syndrómy trichotiodystrofie [c16.131.831.874]
      • xeroderma pigmentosum [c16.131.831.936]

[c16.320.565.100.794]

• 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] +

[c16.320.850.746]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • choroby kožné genetické [c16.320.850] +
      • albinizmus [c16.320.850.080] +
      • cutis laxa [c16.320.850.180]
      • Darierova choroba [c16.320.850.190]
      • dermatitída atopická [c16.320.850.210]
      • dyskeratóza kongenitálna [c16.320.850.235]
      • dysplázia ektodermálna [c16.320.850.250] +
      • Ehlersov-Danlosov syndróm [c16.320.850.260] +
      • epidermolysis bullosa [c16.320.850.275] +
      • erythrokeratodermia variabilis [c16.320.850.337]
      • syndróm hyalínovej fibromatózy [c16.320.850.368]
      • erytroderma ichtyoziformná vrodená [c16.320.850.400] +
      • Siemensova bulózna ichtyóza [c16.320.850.402]
      • ichthyosis vulgaris [c16.320.850.405]
      • ichtyóza viazaná na chromozóm X [c16.320.850.408]
      • incontinentia pigmenti [c16.320.850.420]
      • keratodermia palmoplantárna [c16.320.850.475] +
      • leukokeratóza sliznice, dedičná [c16.320.850.542]
      • Urbachova-Wiethova lipoidproteinóza [c16.320.850.595]
      • monilethrix [c16.320.850.647]
      • Nethertonov syndróm [c16.320.850.673]
      • pemfigus benígny familiárny [c16.320.850.700]
      • porokeratóza [c16.320.850.730]
      • porfýria erytropoetická [c16.320.850.738]
      • porfýrie hepatálne [c16.320.850.742] +
      • deficit prolidázy [c16.320.850.746]
      • pseudoxanthoma elasticum [c16.320.850.750]
      • Rothmundov-Thomsonov syndróm [c16.320.850.765]
      • Sjögrenov-Larssonov syndróm [c16.320.850.820]
      • syndrómy trichotiodystrofie [c16.320.850.895]
      • xeroderma pigmentosum [c16.320.850.970]