Number of the records: 1

Fabryho choroba

	MeSH Tree Structures - Fabryho choroba `[c10.228.140.163.100.435.825.200]` choroby nervového systému [c10] + choroby centrálneho nervového systému [c10.228] + choroby mozgu [c10.228.140] + choroby mozgu, metabolické [c10.228.140.163] + choroby mozgu, metabolické vrodené [c10.228.140.163.100] + choroby lyzozómové, nervového systému [c10.228.140.163.100.435] + sfingolipidózy [c10.228.140.163.100.435.825] + Fabryho choroba `[c10.228.140.163.100.435.825.200]` Farberova lipogranulomatóza [c10.228.140.163.100.435.825.250] gangliozidózy [c10.228.140.163.100.435.825.300] + Gaucherova choroba [c10.228.140.163.100.435.825.400] leukodystrofia globoidocelulárna [c10.228.140.163.100.435.825.590] Niemannove-Pickove choroby [c10.228.140.163.100.435.825.700] + syndróm modrých histiocytov [c10.228.140.163.100.435.825.775] sulfatidóza [c10.228.140.163.100.435.825.850] +
	`[c10.228.140.300.275.374]` choroby nervového systému [c10] + choroby centrálneho nervového systému [c10.228] + choroby mozgu [c10.228.140] + choroby cerebrovaskulárne [c10.228.140.300] + ochorenia malých mozgových ciev [c10.228.140.300.275] + CADASIL [c10.228.140.300.275.249] angiopatia cerebrálna amyloidná familiárna [c10.228.140.300.275.311] Fabryho choroba `[c10.228.140.300.275.374]` MELAS syndróm [c10.228.140.300.275.500] polyangiitída mikroskopická [c10.228.140.300.275.600] infarkt lakunárny [c10.228.140.300.275.800]
	`[c14.907.253.329.374]` choroby kardiovaskulárne [c14] + choroby cievne [c14.907] + choroby cerebrovaskulárne [c14.907.253] + ochorenia malých mozgových ciev [c14.907.253.329] + CADASIL [c14.907.253.329.249] angiopatia cerebrálna amyloidná familiárna [c14.907.253.329.311] Fabryho choroba `[c14.907.253.329.374]` MELAS syndróm [c14.907.253.329.500] polyangiitída mikroskopická [c14.907.253.329.600] infarkt lakunárny [c14.907.253.329.800]
	`[c16.320.322.124]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + choroby genetické, viazané na chromozóm X [c16.320.322] + Aicardiho syndróm [c16.320.322.030] syndróm androgénnej insenzitivity [c16.320.322.061] Barthov syndróm [c16.320.322.068] atrofia bulbospinálna, viazaná na X-chromozóm [c16.320.322.076] chorioiderémia [c16.320.322.092] Dentova choroba [c16.320.322.100] dyskeratóza kongenitálna [c16.320.322.108] dysplázia ektodermálna anhidrotická, typ 1 [c16.320.322.116] Fabryho choroba `[c16.320.322.124]` hypoplázia kože, fokálna [c16.320.322.186] glykogenóza, typ IIb [c16.320.322.201] glykogenóza, typ VIII [c16.320.322.217] choroba granulomatózna chronická [c16.320.322.233] hemofília B [c16.320.322.235] syndróm imunodeficiencie, hyper-IgM, typ 1 [c16.320.322.237] ichtyóza viazaná na chromozóm X [c16.320.322.241] komora ľavá nekompaktná izolovaná [c16.320.322.370] retardácia mentálna viazaná na chromozóm X [c16.320.322.500] + Duchenneova svalová dystrofia [c16.320.322.562] Emeryho-Dreifussova svalová dystrofia [c16.320.322.625] + syndróm okulocerebrorenálny [c16.320.322.750] choroba z deficitu ornitíntranskarbamoylázy [c16.320.322.828] Pelizaeusova-Merzbacherova choroba [c16.320.322.906] Wiskottov-Aldrichov syndróm [c16.320.322.937] imunodeficiencie kombinované, viazané na X-chromozóm [c16.320.322.968]
	`[c16.320.565.189.435.825.200]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + poruchy metabolizmu, vrodené [c16.320.565] + choroby mozgu, metabolické vrodené [c16.320.565.189] + choroby lyzozómové, nervového systému [c16.320.565.189.435] + sfingolipidózy [c16.320.565.189.435.825] + Fabryho choroba `[c16.320.565.189.435.825.200]` Farberova lipogranulomatóza [c16.320.565.189.435.825.250] gangliozidózy [c16.320.565.189.435.825.300] + Gaucherova choroba [c16.320.565.189.435.825.400] leukodystrofia globoidocelulárna [c16.320.565.189.435.825.590] Niemannove-Pickove choroby [c16.320.565.189.435.825.700] + syndróm modrých histiocytov [c16.320.565.189.435.825.775] sulfatidóza [c16.320.565.189.435.825.850] +
	`[c16.320.565.398.641.803.300]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + poruchy metabolizmu, vrodené [c16.320.565] + poruchy metabolizmu lipidov, vrodené [c16.320.565.398] + lipidózy [c16.320.565.398.641] + sfingolipidózy [c16.320.565.398.641.803] + Fabryho choroba `[c16.320.565.398.641.803.300]` Farberova lipogranulomatóza [c16.320.565.398.641.803.325] gangliozidózy [c16.320.565.398.641.803.350] + Gaucherova choroba [c16.320.565.398.641.803.441] leukodystrofia globoidocelulárna [c16.320.565.398.641.803.585] Niemannove-Pickove choroby [c16.320.565.398.641.803.730] + syndróm modrých histiocytov [c16.320.565.398.641.803.850] sulfatidóza [c16.320.565.398.641.803.925] +
	`[c16.320.565.595.554.825.200]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + poruchy metabolizmu, vrodené [c16.320.565] + choroby lyzozómové [c16.320.565.595] + choroby lyzozómové, nervového systému [c16.320.565.595.554] + sfingolipidózy [c16.320.565.595.554.825] + Fabryho choroba `[c16.320.565.595.554.825.200]` Farberova lipogranulomatóza [c16.320.565.595.554.825.250] gangliozidózy [c16.320.565.595.554.825.300] + Gaucherova choroba [c16.320.565.595.554.825.400] leukodystrofia globoidocelulárna [c16.320.565.595.554.825.590] Niemannove-Pickove choroby [c16.320.565.595.554.825.700] + syndróm modrých histiocytov [c16.320.565.595.554.825.775] sulfatidóza [c16.320.565.595.554.825.850] +
	`[c18.452.132.100.435.825.200]` choroby metabolické a poruchy výživy [c18] + choroby metabolické [c18.452] + choroby mozgu, metabolické [c18.452.132] + choroby mozgu, metabolické vrodené [c18.452.132.100] + choroby lyzozómové, nervového systému [c18.452.132.100.435] + sfingolipidózy [c18.452.132.100.435.825] + Fabryho choroba `[c18.452.132.100.435.825.200]` Farberova lipogranulomatóza [c18.452.132.100.435.825.250] gangliozidózy [c18.452.132.100.435.825.300] + Gaucherova choroba [c18.452.132.100.435.825.400] leukodystrofia globoidocelulárna [c18.452.132.100.435.825.590] Niemannove-Pickove choroby [c18.452.132.100.435.825.700] + syndróm modrých histiocytov [c18.452.132.100.435.825.775] sulfatidóza [c18.452.132.100.435.825.850] +
	`[c18.452.584.563.641.803.300]` choroby metabolické a poruchy výživy [c18] + choroby metabolické [c18.452] + poruchy metabolizmu lipidov [c18.452.584] + poruchy metabolizmu lipidov, vrodené [c18.452.584.563] + lipidózy [c18.452.584.563.641] + sfingolipidózy [c18.452.584.563.641.803] + Fabryho choroba `[c18.452.584.563.641.803.300]` Farberova lipogranulomatóza [c18.452.584.563.641.803.325] gangliozidózy [c18.452.584.563.641.803.350] + Gaucherova choroba [c18.452.584.563.641.803.441] leukodystrofia globoidocelulárna [c18.452.584.563.641.803.585] Niemannove-Pickove choroby [c18.452.584.563.641.803.730] + syndróm modrých histiocytov [c18.452.584.563.641.803.850] sulfatidóza [c18.452.584.563.641.803.925] +
	`[c18.452.648.189.435.825.200]` choroby metabolické a poruchy výživy [c18] + choroby metabolické [c18.452] + poruchy metabolizmu, vrodené [c18.452.648] + choroby mozgu, metabolické vrodené [c18.452.648.189] + choroby lyzozómové, nervového systému [c18.452.648.189.435] + sfingolipidózy [c18.452.648.189.435.825] + Fabryho choroba `[c18.452.648.189.435.825.200]` Farberova lipogranulomatóza [c18.452.648.189.435.825.250] gangliozidózy [c18.452.648.189.435.825.300] + Gaucherova choroba [c18.452.648.189.435.825.400] leukodystrofia globoidocelulárna [c18.452.648.189.435.825.590] Niemannove-Pickove choroby [c18.452.648.189.435.825.700] + syndróm modrých histiocytov [c18.452.648.189.435.825.775] sulfatidóza [c18.452.648.189.435.825.850] +
	`[c18.452.648.398.641.803.300]` choroby metabolické a poruchy výživy [c18] + choroby metabolické [c18.452] + poruchy metabolizmu, vrodené [c18.452.648] + poruchy metabolizmu lipidov, vrodené [c18.452.648.398] + lipidózy [c18.452.648.398.641] + sfingolipidózy [c18.452.648.398.641.803] + Fabryho choroba `[c18.452.648.398.641.803.300]` Farberova lipogranulomatóza [c18.452.648.398.641.803.325] gangliozidózy [c18.452.648.398.641.803.350] + Gaucherova choroba [c18.452.648.398.641.803.441] leukodystrofia globoidocelulárna [c18.452.648.398.641.803.585] Niemannove-Pickove choroby [c18.452.648.398.641.803.730] + syndróm modrých histiocytov [c18.452.648.398.641.803.850] sulfatidóza [c18.452.648.398.641.803.925] +
	`[c18.452.648.595.554.825.200]` choroby metabolické a poruchy výživy [c18] + choroby metabolické [c18.452] + poruchy metabolizmu, vrodené [c18.452.648] + choroby lyzozómové [c18.452.648.595] + choroby lyzozómové, nervového systému [c18.452.648.595.554] + sfingolipidózy [c18.452.648.595.554.825] + Fabryho choroba `[c18.452.648.595.554.825.200]` Farberova lipogranulomatóza [c18.452.648.595.554.825.250] gangliozidózy [c18.452.648.595.554.825.300] + Gaucherova choroba [c18.452.648.595.554.825.400] leukodystrofia globoidocelulárna [c18.452.648.595.554.825.590] Niemannove-Pickove choroby [c18.452.648.595.554.825.700] + syndróm modrých histiocytov [c18.452.648.595.554.825.775] sulfatidóza [c18.452.648.595.554.825.850] +

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Number of the records: 1

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