MeSH Tree Structures - Costellov syndróm

[c05.660.207.219]

• 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]

[c16.131.077.256]

• 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]

[c16.320.188]

• choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
  • choroby genetické, vrodené [c16.320] +
    • hyperplázia adrenálna vrodená [c16.320.033]
    • Alagilleov syndróm [c16.320.051]
    • deficit alfa 1-antitrypsínu [c16.320.060]
    • anémia hemolytická vrodená [c16.320.070] +
    • anémia hypoplastická vrodená [c16.320.077] +
    • ataxia teleangiektázia [c16.320.080]
    • syndróm autoimunitný lymfoproliferatívny [c16.320.089]
    • poruchy hemokoagulačné dedičné [c16.320.099] +
    • Brugadov syndróm [c16.320.100]
    • CADASIL [c16.320.129]
    • Camuratiho-Engelmannov syndróm [c16.320.144]
    • kardiomyopatia hypertrofická familiárna [c16.320.160]
    • CHARGE syndróm [c16.320.165]
    • cherubizmus [c16.320.170]
    • poruchy chromozómové [c16.320.180] +
    • ciliopatie [c16.320.184] +
    • Costellov syndróm [c16.320.188]
    • fibróza cystická [c16.320.190]
    • Donohueov syndróm [c16.320.215]
    • nanizmus [c16.320.240] +
    • choroby očné dedičné [c16.320.290] +
    • lipomatóza familiárna mnohopočetná [c16.320.298]
    • Frasierov syndróm [c16.320.306]
    • deficit GATA2 [c16.320.314]
    • choroby genetické, viazané na chromozóm X [c16.320.322] +
    • choroby genetické, viazané na chromozóm Y [c16.320.338]
    • Hajduov-Cheneyho syndróm [c16.320.355]
    • hemoglobinopatie [c16.320.365] +
    • choroby dedičné autozápalové [c16.320.382] +
    • poruchy nervového systému, heredodegeneratívne [c16.320.400] +
    • syndróm imunodeficiencie, hyper-IgM [c16.320.413]
    • hypertyroxinémia familiárna dysalbuminemická [c16.320.427]
    • poruchy imprintingu [c16.320.447] +
    • Kallmannov syndróm [c16.320.467]
    • Kartagenerov syndróm [c16.320.480]
    • laminopatie [c16.320.488] +
    • Lennoxov-Gastautov syndróm [c16.320.495]
    • Loeysov-Dietzov syndróm [c16.320.510]
    • Marfanov syndróm [c16.320.540]
    • poruchy metabolizmu, vrodené [c16.320.565] +
    • dystrofie svalové [c16.320.577] +
    • syndrómy myastenické vrodené [c16.320.590]
    • syndróm necht-jabĺčko [c16.320.600]
    • syndrómy nádorové dedičné [c16.320.700] +
    • syndróm okulocerebrorenálny [c16.320.709]
    • syndrómy orofaciodigitálne [c16.320.714]
    • osteoartropatia primárna hypertrofická [c16.320.718]
    • osteochondrodysplázie [c16.320.728]
    • osteogenesis imperfecta [c16.320.737]
    • necitlivosť na bolesť, vrodená [c16.320.775]
    • Pelgerova-Huetova anomália [c16.320.784]
    • imunodeficiencie primárne [c16.320.798] +
    • pyknodysostóza [c16.320.812]
    • poruchy renálneho tubulárneho transportu, vrodené [c16.320.831] +
    • choroby kožné genetické [c16.320.850] +
    • Wernerov syndróm [c16.320.925]
    • syndróm žltého nechtu [c16.320.962]