Stromová štruktúra MeSH - dysplázia ektodermálna

[c16.131.077.350]

• 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]
        • dysplázia ektodermálna anhidrotická, typ 1 [c16.131.077.350.198]
        • dysplázia ektodermálna anhidrotická, typ 3 [c16.131.077.350.298]
        • dysplázia ektodermálna hypohidrotická, autozomálne recesívna [c16.131.077.350.348]
        • Ellisov-van Creveldov syndróm [c16.131.077.350.398]
        • hypoplázia kože, fokálna [c16.131.077.350.424]
        • dysplázie fokálne dermálne faciálne [c16.131.077.350.568]
        • syndrómy neurokutánne [c16.131.077.350.712]
        • pachyonychia congenita [c16.131.077.350.856]
      • 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]

[c16.131.831.350]

• 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]
        • dysplázia ektodermálna anhidrotická, typ 1 [c16.131.831.350.198]
        • dysplázia ektodermálna anhidrotická, typ 3 [c16.131.831.350.298]
        • dysplázia ektodermálna hypohidrotická, autozomálne recesívna [c16.131.831.350.348]
        • Ellisov-van Creveldov syndróm [c16.131.831.350.398]
        • hypoplázia kože, fokálna [c16.131.831.350.424]
        • dysplázie fokálne dermálne faciálne [c16.131.831.350.568]
        • syndrómy neurokutánne [c16.131.831.350.712]
        • pachyonychia congenita [c16.131.831.350.856] +
      • 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]

[c16.320.850.250]

• 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]
        • dysplázia ektodermálna anhidrotická, typ 1 [c16.320.850.250.198]
        • dysplázia ektodermálna anhidrotická, typ 3 [c16.320.850.250.298]
        • dysplázia ektodermálna hypohidrotická, autozomálne recesívna [c16.320.850.250.348]
        • Ellisov-van Creveldov syndróm [c16.320.850.250.398]
        • hypoplázia kože, fokálna [c16.320.850.250.424]
        • dysplázie fokálne dermálne faciálne [c16.320.850.250.568]
        • syndrómy neurokutánne [c16.320.850.250.712]
        • pachyonychia congenita [c16.320.850.250.856] +
      • 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]

[c17.800.804.350]

• choroby kože a spojivového tkaniva [c17] +
  • choroby kožné [c17.800] +
    • abnormality kožné [c17.800.804] +
      • akrodermatitída [c17.800.804.066]
      • Anetoderma [c17.800.804.108]
      • dyskeratóza kongenitálna [c17.800.804.150]
      • dysplázia ektodermálna [c17.800.804.350]
        • dysplázia ektodermálna anhidrotická, typ 1 [c17.800.804.350.198]
        • dysplázia ektodermálna anhidrotická, typ 3 [c17.800.804.350.298]
        • dysplázia ektodermálna hypohidrotická, autozomálne recesívna [c17.800.804.350.348]
        • Ellisov-van Creveldov syndróm [c17.800.804.350.398]
        • hypoplázia kože, fokálna [c17.800.804.350.424]
        • dysplázie fokálne dermálne faciálne [c17.800.804.350.568]
        • syndrómy neurokutánne [c17.800.804.350.712]
        • pachyonychia congenita [c17.800.804.350.856] +
      • Ehlersov-Danlosov syndróm [c17.800.804.428] +
      • epidermolysis bullosa [c17.800.804.493] +
      • ichtyóza [c17.800.804.512] +
      • incontinentia pigmenti [c17.800.804.580]
      • naevus flammeus [c17.800.804.675]
      • pseudoxanthoma elasticum [c17.800.804.766]
      • Rothmundov-Thomsonov syndróm [c17.800.804.775]
      • scleredema neonatorum [c17.800.804.812]
      • syndrómy trichotiodystrofie [c17.800.804.874]
      • xeroderma pigmentosum [c17.800.804.936]

[c17.800.827.250]

• 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]
        • dysplázia ektodermálna anhidrotická, typ 1 [c17.800.827.250.198]
        • dysplázia ektodermálna anhidrotická, typ 3 [c17.800.827.250.298]
        • dysplázia ektodermálna hypohidrotická, autozomálne recesívna [c17.800.827.250.348]
        • Ellisov-van Creveldov syndróm [c17.800.827.250.398]
        • hypoplázia kože, fokálna [c17.800.827.250.424]
        • dysplázie fokálne dermálne faciálne [c17.800.827.250.568]
        • syndrómy neurokutánne [c17.800.827.250.712]
        • pachyonychia congenita [c17.800.827.250.856] +
      • 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]