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1.albinizmus

	MeSH Tree Structures - albinizmus `[c11.270.040]` choroby očné [c11] + choroby očné dedičné [c11.270] + Aicardiho syndróm [c11.270.019] albinizmus `[c11.270.040]` albinizmus očný [c11.270.040.090] albinizmus okulokutánny [c11.270.040.545] + Chédiakov-Higashiho syndróm [c11.270.040.772] + anirídia [c11.270.060] + chorioiderémia [c11.270.142] kolobóm [c11.270.147] + dystrofia čapíkov [c11.270.151] + dystrofie tyčiniek a čapíkov [c11.270.152] dystrofia rohovky, dedičná [c11.270.162] + Duaneov syndróm retrakcie [c11.270.235] vitreoretinopatie exsudatívne familiárne [c11.270.238] Gravesova oftalmopatia [c11.270.240] atrofia gyrata [c11.270.468] Leberova kongenitálna amauróza [c11.270.516] atrofie zrakového nervu, dedičné [c11.270.564] + hypoplázia zrakového nervu [c11.270.588] degenerácia sietnice [c11.270.612] dysplázia sietnice [c11.270.660] retinitis pigmentosa [c11.270.684] + retinoblastóm [c11.270.862] Stargardtova choroba [c11.270.872] Walkerov-Warburgov syndróm [c11.270.881] Weillov-Marchesaniho syndróm [c11.270.921]
	`[c16.320.290.040]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + choroby očné dedičné [c16.320.290] + Aicardiho syndróm [c16.320.290.019] albinizmus `[c16.320.290.040]` albinizmus očný [c16.320.290.040.090] albinizmus okulokutánny [c16.320.290.040.100] + piebaldizmus [c16.320.290.040.600] anirídia [c16.320.290.078] + chorioiderémia [c16.320.290.142] dystrofie tyčiniek a čapíkov [c16.320.290.152] dystrofia rohovky, dedičná [c16.320.290.162] + Duaneov syndróm retrakcie [c16.320.290.235] vitreoretinopatie exsudatívne familiárne [c16.320.290.352] Gravesova oftalmopatia [c16.320.290.410] atrofia gyrata [c16.320.290.468] atrofie zrakového nervu, dedičné [c16.320.290.564] + hypoplázia zrakového nervu [c16.320.290.612] dysplázia sietnice [c16.320.290.660] retinitis pigmentosa [c16.320.290.684] + Stargardtova choroba [c16.320.290.724] dystrofia makuly, viteliformná [c16.320.290.763] Weillov-Marchesaniho syndróm [c16.320.290.842]
	`[c16.320.565.100.102]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + poruchy metabolizmu, vrodené [c16.320.565] + poruchy metabolizmu aminokyselín, vrodené [c16.320.565.100] + albinizmus `[c16.320.565.100.102]` albinizmus očný [c16.320.565.100.102.090] albinizmus okulokutánny [c16.320.565.100.102.100] + piebaldizmus [c16.320.565.100.102.600] alkaptonúria [c16.320.565.100.187] hyperglycinémia neketotická [c16.320.565.100.477] hyperhomocysteinémia [c16.320.565.100.480] + hyperlyzinémie [c16.320.565.100.544] leucinóza [c16.320.565.100.608] deficit acyl-CoA dehydrogenázy, mnohopočetný [c16.320.565.100.614] deficit karboxylázy, mnohopočetný [c16.320.565.100.620] + fenylketonúrie [c16.320.565.100.766] + deficit prolidázy [c16.320.565.100.794] acidémia propiónová [c16.320.565.100.823] tyrozinémie [c16.320.565.100.880] poruchy močovinového cyklu, vrodené [c16.320.565.100.940] +
	`[c16.320.850.080]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + choroby kožné genetické [c16.320.850] + albinizmus `[c16.320.850.080]` albinizmus očný [c16.320.850.080.090] albinizmus okulokutánny [c16.320.850.080.100] + piebaldizmus [c16.320.850.080.600] 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]
	`[c17.800.621.440.102]` choroby kože a spojivového tkaniva [c17] + choroby kožné [c17.800] + poruchy pigmentácie [c17.800.621] + hypopigmentácia [c17.800.621.440] + albinizmus `[c17.800.621.440.102]` albinizmus očný [c17.800.621.440.102.090] albinizmus okulokutánny [c17.800.621.440.102.100] + piebaldizmus [c17.800.621.440.102.600] vitiligo [c17.800.621.440.895]
	`[c17.800.827.080]` choroby kože a spojivového tkaniva [c17] + choroby kožné [c17.800] + choroby kožné genetické [c17.800.827] + albinizmus `[c17.800.827.080]` albinizmus očný [c17.800.827.080.090] albinizmus okulokutánny [c17.800.827.080.100] + piebaldizmus [c17.800.827.080.600] 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]
	`[c18.452.648.100.102]` choroby metabolické a poruchy výživy [c18] + choroby metabolické [c18.452] + poruchy metabolizmu, vrodené [c18.452.648] + poruchy metabolizmu aminokyselín, vrodené [c18.452.648.100] + albinizmus `[c18.452.648.100.102]` albinizmus očný [c18.452.648.100.102.090] albinizmus okulokutánny [c18.452.648.100.102.100] + piebaldizmus [c18.452.648.100.102.600] alkaptonúria [c18.452.648.100.187] hyperglycinémia neketotická [c18.452.648.100.477] hyperhomocysteinémia [c18.452.648.100.480] + hyperlyzinémie [c18.452.648.100.544] leucinóza [c18.452.648.100.608] deficit acyl-CoA dehydrogenázy, mnohopočetný [c18.452.648.100.614] deficit karboxylázy, mnohopočetný [c18.452.648.100.620] + fenylketonúrie [c18.452.648.100.766] + acidémia propiónová [c18.452.648.100.823] tyrozinémie [c18.452.648.100.880] poruchy močovinového cyklu, vrodené [c18.452.648.100.940] +

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