Number of the records: 1

deficit prolidázy

	MeSH Tree Structures - deficit prolidázy `[c16.131.077.735]` 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]
	`[c16.131.831.720]` 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] + 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]
	`[c16.320.565.100.794]` 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] + 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] +
	`[c16.320.850.746]` 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] + 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]

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Number of the records: 1

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