Number of the records: 1

Ehlersov-Danlosov syndróm

	MeSH Tree Structures - Ehlersov-Danlosov syndróm `[c14.907.454.240]` choroby kardiovaskulárne [c14] + choroby cievne [c14.907] + poruchy hemostázy [c14.907.454] + kryoglobulinémia [c14.907.454.140] Ehlersov-Danlosov syndróm `[c14.907.454.240]` Ehlersov-Danlosov syndróm IV. typu [c14.907.454.240.500] hemangióm kavernózny [c14.907.454.385] + myelóm mnohopočetný [c14.907.454.460] pseudoxanthoma elasticum [c14.907.454.530] purpura hyperglobulinemická [c14.907.454.550] skorbut [c14.907.454.800] Shwartzmanov fenomén [c14.907.454.810] teleangiektázia dedičná hemoragická [c14.907.454.900] Waldenströmova makroglobulinémia [c14.907.454.960]
	`[c15.378.463.515.240]` choroby krvné a lymfatické [c15] + choroby hematologické [c15.378] + poruchy hemoragické [c15.378.463] + poruchy hemostázy [c15.378.463.515] + kryoglobulinémia [c15.378.463.515.140] Ehlersov-Danlosov syndróm `[c15.378.463.515.240]` Ehlersov-Danlosov syndróm IV. typu [c15.378.463.515.240.500] hemangióm kavernózny [c15.378.463.515.385] + myelóm mnohopočetný [c15.378.463.515.460] pseudoxanthoma elasticum [c15.378.463.515.530] purpura hyperglobulinemická [c15.378.463.515.550] IgA vaskulitída [c15.378.463.515.580] skorbut [c15.378.463.515.800] Shwartzmanov fenomén [c15.378.463.515.810] teleangiektázia dedičná hemoragická [c15.378.463.515.900] Waldenströmova makroglobulinémia [c15.378.463.515.960]
	`[c16.131.831.428]` 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]` Ehlersov-Danlosov syndróm IV. typu [c16.131.831.428.500] 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]
	`[c16.320.850.260]` 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]` Ehlersov-Danlosov syndróm IV. typu [c16.320.850.260.500] 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]
	`[c17.300.200.310]` choroby kože a spojivového tkaniva [c17] + choroby spojivového tkaniva [c17.300] + kolagenózy [c17.300.200] + Ehlersov-Danlosov syndróm `[c17.300.200.310]` Ehlersov-Danlosov syndróm IV. typu [c17.300.200.310.500] epidermolysis bullosa dystrophica [c17.300.200.367] keloid [c17.300.200.425] + poruchy nekrobiotické [c17.300.200.495] + nefritída dedičná [c17.300.200.517] osteogenesis imperfecta [c17.300.200.540]
	`[c17.800.804.428]` choroby kože a spojivového tkaniva [c17] + choroby kožné [c17.800] + abnormality kožné [c17.800.804] + akrodermatitída [c17.800.804.066] Anetoderma [c17.800.804.108] dyskeratóza kongenitálna [c17.800.804.150] dysplázia ektodermálna [c17.800.804.350] + Ehlersov-Danlosov syndróm `[c17.800.804.428]` Ehlersov-Danlosov syndróm IV. typu [c17.800.804.428.500] epidermolysis bullosa [c17.800.804.493] + ichtyóza [c17.800.804.512] + incontinentia pigmenti [c17.800.804.580] naevus flammeus [c17.800.804.675] pseudoxanthoma elasticum [c17.800.804.766] Rothmundov-Thomsonov syndróm [c17.800.804.775] scleredema neonatorum [c17.800.804.812] syndrómy trichotiodystrofie [c17.800.804.874] xeroderma pigmentosum [c17.800.804.936]
	`[c17.800.827.260]` choroby kože a spojivového tkaniva [c17] + choroby kožné [c17.800] + choroby kožné genetické [c17.800.827] + albinizmus [c17.800.827.080] + 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]` Ehlersov-Danlosov syndróm IV. typu [c17.800.827.260.500] 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]

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Number of the records: 1

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