Stromová štruktúra MeSH - leukokeratóza sliznice, dedičná

[c16.320.850.542]

• 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]

[c17.800.827.595]

• choroby kože a spojivového tkaniva [c17] +
  • choroby kožné [c17.800] +
    • choroby kožné genetické [c17.800.827] +
      • albinizmus [c17.800.827.080] +
      • cutis laxa [c17.800.827.180]
      • Darierova choroba [c17.800.827.190]
      • dermatitída atopická [c17.800.827.210]
      • dyskeratóza kongenitálna [c17.800.827.235]
      • dysplázia ektodermálna [c17.800.827.250] +
      • Ehlersov-Danlosov syndróm [c17.800.827.260] +
      • epidermolysis bullosa [c17.800.827.275] +
      • erythrokeratodermia variabilis [c17.800.827.337]
      • choroby dedičné autozápalové [c17.800.827.368] +
      • syndróm hyalínovej fibromatózy [c17.800.827.384]
      • erytroderma ichtyoziformná vrodená [c17.800.827.400] +
      • Siemensova bulózna ichtyóza [c17.800.827.403]
      • ichthyosis vulgaris [c17.800.827.405]
      • ichtyóza viazaná na chromozóm X [c17.800.827.408]
      • incontinentia pigmenti [c17.800.827.420]
      • keratodermia palmoplantárna [c17.800.827.475] +
      • leukokeratóza sliznice, dedičná [c17.800.827.595]
      • monilethrix [c17.800.827.602]
      • Muirov-Torreho syndróm [c17.800.827.610]
      • Nethertonov syndróm [c17.800.827.655]
      • pemfigus benígny familiárny [c17.800.827.700]
      • porokeratóza [c17.800.827.730]
      • porfýria erytropoetická [c17.800.827.738]
      • porfýrie hepatálne [c17.800.827.742] +
      • pseudoxanthoma elasticum [c17.800.827.750]
      • Rothmundov-Thomsonov syndróm [c17.800.827.775]
      • Sjögrenov-Larssonov syndróm [c17.800.827.820]
      • syndrómy trichotiodystrofie [c17.800.827.895]
      • xeroderma pigmentosum [c17.800.827.970]