Number of the records: 1

Alagillov syndróm

	MeSH Tree Structures - Alagillov syndróm `[c06.130.120.135.250.125]` choroby tráviaceho systému [c06] + choroby žlčového systému [c06.130] + choroby žlčových ciest [c06.130.120] + cholestáza [c06.130.120.135] + cholestáza intrahepatálna [c06.130.120.135.250] + Alagillov syndróm `[c06.130.120.135.250.125]` cirhóza pečene, biliárna [c06.130.120.135.250.250]
	`[c06.552.150.125]` choroby tráviaceho systému [c06] + choroby pečene [c06.552] + cholestáza intrahepatálna [c06.552.150] + Alagillov syndróm `[c06.552.150.125]` cirhóza pečene, biliárna [c06.552.150.250]
	`[c14.240.400.044]` choroby kardiovaskulárne [c14] + abnormality kardiovaskulárne [c14.240] + chyby srdcové vrodené [c14.240.400] + syndróm delécie 22q11 [c14.240.400.021] + Alagillov syndróm `[c14.240.400.044]` koarktácia aorty [c14.240.400.090] tunel aorto-ventrikulárny [c14.240.400.118] dysplázia pravej komory, arytmogénna [c14.240.400.145] Barthov syndróm [c14.240.400.172] choroba bikuspidálnej aortálnej chlopne [c14.240.400.186] cor triatriatum [c14.240.400.200] anomálie koronárnych ciev [c14.240.400.210] + transpozícia ciev srdca [c14.240.400.220] dextrokardia [c14.240.400.280] + ductus arteriosus patens [c14.240.400.340] Ebsteinova anomália [c14.240.400.395] ektopia srdca [c14.240.400.422] Eisenmengerov komplex [c14.240.400.450] defekty srdcového septa [c14.240.400.560] + syndróm heterotaxie [c14.240.400.592] syndróm hypoplázie ľavého srdca [c14.240.400.625] komora ľavá nekompaktná izolovaná [c14.240.400.660] LEOPARD-syndróm [c14.240.400.695] levokardia [c14.240.400.701] Marfanov syndróm [c14.240.400.725] Noonanovej syndróm [c14.240.400.787] chlopňa aortálna štvorcípa [c14.240.400.818] Fallotova tetralógia [c14.240.400.849] transpozícia veľkých ciev [c14.240.400.915] + atrézia trojcípej chlopne [c14.240.400.920] Fallotova trilógia [c14.240.400.960] syndróm trizómie 13 [c14.240.400.970] syndróm trizómie 18 [c14.240.400.975] Turnerov syndróm [c14.240.400.980] srdce univentrikulárne [c14.240.400.990]
	`[c16.131.077.065]` 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]
	`[c16.131.240.400.044]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + abnormality vrodené [c16.131] + abnormality kardiovaskulárne [c16.131.240] + chyby srdcové vrodené [c16.131.240.400] + syndróm delécie 22q11 [c16.131.240.400.021] + Alagillov syndróm `[c16.131.240.400.044]` koarktácia aorty [c16.131.240.400.090] tunel aorto-ventrikulárny [c16.131.240.400.118] dysplázia pravej komory, arytmogénna [c16.131.240.400.145] Barthov syndróm [c16.131.240.400.172] choroba bikuspidálnej aortálnej chlopne [c16.131.240.400.186] cor triatriatum [c16.131.240.400.200] anomálie koronárnych ciev [c16.131.240.400.210] + transpozícia ciev srdca [c16.131.240.400.220] dextrokardia [c16.131.240.400.280] + ductus arteriosus patens [c16.131.240.400.340] Ebsteinova anomália [c16.131.240.400.395] ektopia srdca [c16.131.240.400.422] Eisenmengerov komplex [c16.131.240.400.450] defekty srdcového septa [c16.131.240.400.560] + syndróm heterotaxie [c16.131.240.400.592] syndróm hypoplázie ľavého srdca [c16.131.240.400.625] komora ľavá nekompaktná izolovaná [c16.131.240.400.655] LEOPARD-syndróm [c16.131.240.400.685] levokardia [c16.131.240.400.701] syndróm dlhého QT intervalu [c16.131.240.400.715] + Marfanov syndróm [c16.131.240.400.720] Noonanovej syndróm [c16.131.240.400.784] chlopňa aortálna štvorcípa [c16.131.240.400.817] Fallotova tetralógia [c16.131.240.400.849] transpozícia veľkých ciev [c16.131.240.400.915] + atrézia trojcípej chlopne [c16.131.240.400.920] Fallotova trilógia [c16.131.240.400.960] syndróm trizómie 13 [c16.131.240.400.965] syndróm trizómie 18 [c16.131.240.400.968] Turnerov syndróm [c16.131.240.400.970] srdce univentrikulárne [c16.131.240.400.975] Wolffov-Parkinsonov-Whiteov syndróm [c16.131.240.400.980]
	`[c16.320.051]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + hyperplázia adrenálna vrodená [c16.320.033] Alagillov 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]

subject heading

subject heading

Number of the records: 1

For full functionality of this site it is necessary to enable JavaScript. Here are the instructions how to enable JavaScript in your web browser.