Stromová štruktúra MeSH - Silverov-Russellov syndróm

[c05.660.207.925]

• choroby muskuloskeletárne [c05] +
  • abnormality muskuloskeletárne [c05.660] +
    • abnormality kraniofaciálne [c05.660.207] +
      • syndróm delécie 22q11 [c05.660.207.103] +
      • dysplázia kleidokraniálna [c05.660.207.207]
      • Costellov syndróm [c05.660.207.219]
      • dyzostóza kraniofaciálna [c05.660.207.231] +
      • kraniosynostózy [c05.660.207.240] +
      • Donohueov syndróm [c05.660.207.325]
      • holoprozencefália [c05.660.207.410]
      • LEOPARD-syndróm [c05.660.207.525]
      • Loeysov-Dietzov syndróm [c05.660.207.532]
      • megalencefália [c05.660.207.536] +
      • abnormality maxilofaciálne [c05.660.207.540] +
      • mikrocefália [c05.660.207.620] +
      • Noonanovej syndróm [c05.660.207.690]
      • syndrómy orofaciodigitálne [c05.660.207.700]
      • plagiocefália [c05.660.207.707] +
      • platybázia [c05.660.207.720]
      • Rubinsteinov-Taybiho syndróm [c05.660.207.850]
      • Silverov-Russellov syndróm [c05.660.207.925]

[c16.131.077.855]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • abnormality vrodené [c16.131] +
    • abnormality mnohopočetné [c16.131.077] +
      • syndróm delécie 22q11 [c16.131.077.019] +
      • Alagilleov 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]

[c16.131.260.870]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • abnormality vrodené [c16.131] +
    • poruchy chromozómové [c16.131.260] +
      • syndróm delécie 22q11 [c16.131.260.019] +
      • Angelmanov syndróm [c16.131.260.040]
      • Beckwithov-Wiedemannov syndróm [c16.131.260.080]
      • syndróm branchiootorenálny [c16.131.260.090]
      • cri-du-chat syndróm [c16.131.260.190]
      • de Langeovej syndróm [c16.131.260.210]
      • Downov syndróm [c16.131.260.260]
      • holoprozencefália [c16.131.260.380]
      • Jacobsenov syndróm distálnej delécie 11q [c16.131.260.440]
      • Praderovej-Williho syndróm [c16.131.260.700]
      • Rubinsteinov-Taybiho syndróm [c16.131.260.790]
      • poruchy spôsobené aberáciami pohlavných chromozómov [c16.131.260.830] +
      • Silverov-Russellov syndróm [c16.131.260.870]
      • Smithovej-Magenisovej syndróm [c16.131.260.887]
      • Sotosov syndróm [c16.131.260.905]
      • syndróm trizómie 13 [c16.131.260.923]
      • syndróm trizómie 18 [c16.131.260.932]
      • WAGR syndróm [c16.131.260.940]
      • Williamsov syndróm [c16.131.260.970]
      • Wolfov-Hirschhornov syndróm [c16.131.260.985]

[c16.320.180.870]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • poruchy chromozómové [c16.320.180] +
      • syndróm delécie 22q11 [c16.320.180.019] +
      • Angelmanov syndróm [c16.320.180.040]
      • Beckwithov-Wiedemannov syndróm [c16.320.180.080]
      • syndróm branchiootorenálny [c16.320.180.090]
      • cri-du-chat syndróm [c16.320.180.190]
      • de Langeovej syndróm [c16.320.180.210]
      • Downov syndróm [c16.320.180.260]
      • holoprozencefália [c16.320.180.380]
      • Jacobsenov syndróm distálnej delécie 11q [c16.320.180.440]
      • Praderovej-Williho syndróm [c16.320.180.700]
      • Rubinsteinov-Taybiho syndróm [c16.320.180.790]
      • poruchy spôsobené aberáciami pohlavných chromozómov [c16.320.180.830] +
      • Silverov-Russellov syndróm [c16.320.180.870]
      • Smithovej-Magenisovej syndróm [c16.320.180.887]
      • Sotosov syndróm [c16.320.180.905]
      • syndróm trizómie 13 [c16.320.180.923]
      • syndróm trizómie 18 [c16.320.180.932]
      • WAGR syndróm [c16.320.180.940]
      • Williamsov syndróm [c16.320.180.970]
      • Wolfov-Hirschhornov syndróm [c16.320.180.985]

[c16.320.240.937]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • nanizmus [c16.320.240] +
      • achondroplázia [c16.320.240.500] +
      • Cockayneov syndróm [c16.320.240.562]
      • hypotyreóza vrodená [c16.320.240.625]
      • Laronov syndróm [c16.320.240.750]
      • nanizmus mulibrey [c16.320.240.875]
      • Silverov-Russellov syndróm [c16.320.240.937]

[c16.320.447.750]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • poruchy imprintingu [c16.320.447] +
      • Angelmanov syndróm [c16.320.447.250]
      • Beckwithov-Wiedemannov syndróm [c16.320.447.375]
      • Praderovej-Williho syndróm [c16.320.447.500]
      • Silverov-Russellov syndróm [c16.320.447.750]

Stromová štruktúra MeSH - prietrž pupočná

[c16.614.378]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby novorodencov [c16.614] +
    • syndróm amniálnych pruhov [c16.614.042]
    • anémia novorodenecká [c16.614.053] +
    • asfyxia novorodencov [c16.614.092]
    • poranenia pôrodné u novorodencov [c16.614.131] +
    • kolika [c16.614.166]
    • syndrómy zlyhania kostnej drene, vrodené [c16.614.183]
    • hyperinzulinizmus vrodený [c16.614.200] +
    • fibróza cystická [c16.614.213]
    • epilepsia novorodenecká benígna [c16.614.258]
    • erytroblastóza fetálna [c16.614.304] +
    • prietrž pupočná [c16.614.378]
    • hydroftalmus [c16.614.438]
    • hyperbilirubinémia novorodenecká [c16.614.451] +
    • hyperostóza kôrová vrodená [c16.614.465]
    • ichtyóza [c16.614.492] +
    • choroby nezrelých novorodencov [c16.614.521] +
    • syndróm aspirácie mekónia [c16.614.580]
    • Mobiov syndróm [c16.614.595]
    • syndróm abstinenčný, u novorodencov [c16.614.610]
    • sepsa novorodenecká [c16.614.627]
    • nystagmus vrodený [c16.614.643]
    • ophthalmia neonatorum [c16.614.677]
    • syndróm pretrvávajúceho fetálneho obehu [c16.614.694]
    • Rothmundov-Thomsonov syndróm [c16.614.760]
    • scleredema neonatorum [c16.614.810]
    • imunodeficiencia kombinovaná ťažká [c16.614.815] +
    • syfilis vrodený [c16.614.868]
    • dysplázia tanatoforická [c16.614.890]
    • trombocytopénia novorodenecká aloimunitná [c16.614.899]
    • toxoplazmóza vrodená [c16.614.909]
    • krvácanie z nedostatku vitamínu K [c16.614.940]
    • Wolmanova choroba [c16.614.947]

[c23.300.707.374.937.500]

• stavy patologické, príznaky a symptómy [c23] +
  • nálezy patologicko-anatomické [c23.300] +
    • prietrž [c23.300.707] +
      • prietrž brušná [c23.300.707.374] +
        • prietrž ventrálna [c23.300.707.374.937] +
          • prietrž pupočná [c23.300.707.374.937.500]

Stromová štruktúra MeSH - gény Wilmsovho nádoru

[g05.360.340.024.340.375.249.420]

• javy genetické [g05] +
  • štruktúry genetické [g05.360] +
    • genóm [g05.360.340] +
      • časti genómu [g05.360.340.024] +
        • gény [g05.360.340.024.340] +
          • gény nádorové [g05.360.340.024.340.375] +
            • gény supresorové nádorové [g05.360.340.024.340.375.249] +
              • gény APC [g05.360.340.024.340.375.249.050]
              • gény BRCA1 [g05.360.340.024.340.375.249.100]
              • gény BRCA2 [g05.360.340.024.340.375.249.105]
              • gény DCC [g05.360.340.024.340.375.249.200]
              • gény MCC [g05.360.340.024.340.375.249.320]
              • gény neurofibromatózy 1 [g05.360.340.024.340.375.249.340]
              • gény neurofibromatózy 2 [g05.360.340.024.340.375.249.345]
              • gény p16 [g05.360.340.024.340.375.249.375]
              • gény p53 [g05.360.340.024.340.375.249.385]
              • gény retinoblastómu [g05.360.340.024.340.375.249.400]
              • gény Wilmsovho nádoru [g05.360.340.024.340.375.249.420]

[g05.360.340.024.340.415.400.420]

• javy genetické [g05] +
  • štruktúry genetické [g05.360] +
    • genóm [g05.360.340] +
      • časti genómu [g05.360.340.024] +
        • gény [g05.360.340.024.340] +
          • gény recesívne [g05.360.340.024.340.415] +
            • gény supresorové nádorové [g05.360.340.024.340.415.400] +
              • gény APC [g05.360.340.024.340.415.400.050]
              • gény BRCA1 [g05.360.340.024.340.415.400.100]
              • gény BRCA2 [g05.360.340.024.340.415.400.105]
              • gény DCC [g05.360.340.024.340.415.400.200]
              • gény MCC [g05.360.340.024.340.415.400.320]
              • gény neurofibromatózy 1 [g05.360.340.024.340.415.400.340]
              • gény neurofibromatózy 2 [g05.360.340.024.340.415.400.345]
              • gény p16 [g05.360.340.024.340.415.400.375]
              • gény p53 [g05.360.340.024.340.415.400.385]
              • gény retinoblastómu [g05.360.340.024.340.415.400.400]
              • gény Wilmsovho nádoru [g05.360.340.024.340.415.400.420]