Number of the records: 1

Leschov-Nyhanov syndróm

	MeSH Tree Structures - Leschov-Nyhanov syndróm `[c10.228.140.163.100.425]` 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] + adrenoleukodystrofia [c10.228.140.163.100.084] angiopatia cerebrálna amyloidná familiárna [c10.228.140.163.100.168] galaktozémie [c10.228.140.163.100.320] Hartnupova choroba [c10.228.140.163.100.355] degenerácia hepatolentikulárna [c10.228.140.163.100.360] choroby centrálneho nervového systému demyelinizačné, dedičné [c10.228.140.163.100.362] + homocystinúria [c10.228.140.163.100.365] hyperglycinémia neketotická [c10.228.140.163.100.375] hyperlyzinémie [c10.228.140.163.100.380] Leighov syndróm [c10.228.140.163.100.412] Leschov-Nyhanov syndróm `[c10.228.140.163.100.425]` choroby lyzozómové, nervového systému [c10.228.140.163.100.435] + leucinóza [c10.228.140.163.100.520] MELAS syndróm [c10.228.140.163.100.535] Menkesov syndróm [c10.228.140.163.100.540] MERRF syndróm [c10.228.140.163.100.545] deficit mevalonátkinázy [c10.228.140.163.100.593] syndróm okulocerebrorenálny [c10.228.140.163.100.640] fenylketonúrie [c10.228.140.163.100.687] + choroba z deficitu pyruvátkarboxylázy [c10.228.140.163.100.725] choroba z deficitu pyruvátdehydrogenázového komplexu [c10.228.140.163.100.750] Refsumova choroba [c10.228.140.163.100.813] Refsumova choroba, infantilný typ [c10.228.140.163.100.844] tyrozinémie [c10.228.140.163.100.875] poruchy močovinového cyklu, vrodené [c10.228.140.163.100.937] + Zellwegerov syndróm [c10.228.140.163.100.968]
	`[c10.597.606.360.455.625]` choroby nervového systému [c10] + symptómy neurologické [c10.597] + symptómy neurobehaviorálne [c10.597.606] + postihnutie intelektuálne [c10.597.606.360] + retardácia mentálna viazaná na chromozóm X [c10.597.606.360.455] + adrenoleukodystrofia [c10.597.606.360.455.124] Coffinov-Lowryho syndróm [c10.597.606.360.455.249] syndróm fragilného chromozómu X [c10.597.606.360.455.500] glykogenóza, typ IIb [c10.597.606.360.455.562] Leschov-Nyhanov syndróm `[c10.597.606.360.455.625]` Menkesov syndróm [c10.597.606.360.455.687] mukopolysacharidóza II [c10.597.606.360.455.750] choroba z deficitu pyruvátdehydrogenázového komplexu [c10.597.606.360.455.875] Rettov syndróm [c10.597.606.360.455.937]
	`[c16.320.322.500.625]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + choroby genetické, viazané na chromozóm X [c16.320.322] + retardácia mentálna viazaná na chromozóm X [c16.320.322.500] + adrenoleukodystrofia [c16.320.322.500.124] lissencefálie klasické a heterotopie subkortikálne pruhovité [c16.320.322.500.186] Coffinov-Lowryho syndróm [c16.320.322.500.249] syndróm fragilného chromozómu X [c16.320.322.500.500] Leschov-Nyhanov syndróm `[c16.320.322.500.625]` Menkesov syndróm [c16.320.322.500.687] mukopolysacharidóza II [c16.320.322.500.750] choroba z deficitu pyruvátdehydrogenázového komplexu [c16.320.322.500.875] Rettov syndróm [c16.320.322.500.937]
	`[c16.320.400.525.625]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + poruchy nervového systému, heredodegeneratívne [c16.320.400] + retardácia mentálna viazaná na chromozóm X [c16.320.400.525] + adrenoleukodystrofia [c16.320.400.525.124] Coffinov-Lowryho syndróm [c16.320.400.525.249] syndróm fragilného chromozómu X [c16.320.400.525.500] Leschov-Nyhanov syndróm `[c16.320.400.525.625]` Menkesov syndróm [c16.320.400.525.687] mukopolysacharidóza II [c16.320.400.525.750] choroba z deficitu pyruvátdehydrogenázového komplexu [c16.320.400.525.875] Rettov syndróm [c16.320.400.525.937]
	`[c16.320.565.189.425]` 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] + adrenoleukodystrofia [c16.320.565.189.084] angiopatia cerebrálna amyloidná familiárna [c16.320.565.189.168] galaktozémie [c16.320.565.189.320] Hartnupova choroba [c16.320.565.189.355] degenerácia hepatolentikulárna [c16.320.565.189.360] choroby centrálneho nervového systému demyelinizačné, dedičné [c16.320.565.189.362] + homocystinúria [c16.320.565.189.365] hyperglycinémia neketotická [c16.320.565.189.375] hyperlyzinémie [c16.320.565.189.380] Leighov syndróm [c16.320.565.189.412] Leschov-Nyhanov syndróm `[c16.320.565.189.425]` choroby lyzozómové, nervového systému [c16.320.565.189.435] + leucinóza [c16.320.565.189.520] MELAS syndróm [c16.320.565.189.535] Menkesov syndróm [c16.320.565.189.540] MERRF syndróm [c16.320.565.189.545] deficit mevalonátkinázy [c16.320.565.189.593] syndróm okulocerebrorenálny [c16.320.565.189.640] fenylketonúrie [c16.320.565.189.687] + choroba z deficitu pyruvátkarboxylázy [c16.320.565.189.725] choroba z deficitu pyruvátdehydrogenázového komplexu [c16.320.565.189.750] Refsumova choroba [c16.320.565.189.813] Refsumova choroba, infantilný typ [c16.320.565.189.844] tyrozinémie [c16.320.565.189.875] poruchy močovinového cyklu, vrodené [c16.320.565.189.937] + Zellwegerov syndróm [c16.320.565.189.968]
	`[c16.320.565.798.594]` choroby a abnormality novorodenecké, vrodené a dedičné [c16] + choroby genetické, vrodené [c16.320] + poruchy metabolizmu, vrodené [c16.320.565] + poruchy metabolizmu purínu a pyrimidínu, vrodené [c16.320.565.798] + deficit dihydropyrimidíndehydrogenázy [c16.320.565.798.183] dna (choroba) [c16.320.565.798.368] + Leschov-Nyhanov syndróm `[c16.320.565.798.594]`
	`[c18.452.132.100.425]` choroby metabolické a poruchy výživy [c18] + choroby metabolické [c18.452] + choroby mozgu, metabolické [c18.452.132] + choroby mozgu, metabolické vrodené [c18.452.132.100] + adrenoleukodystrofia [c18.452.132.100.084] angiopatia cerebrálna amyloidná familiárna [c18.452.132.100.168] galaktozémie [c18.452.132.100.320] Hartnupova choroba [c18.452.132.100.355] degenerácia hepatolentikulárna [c18.452.132.100.360] choroby centrálneho nervového systému demyelinizačné, dedičné [c18.452.132.100.362] + homocystinúria [c18.452.132.100.365] hyperglycinémia neketotická [c18.452.132.100.375] hyperlyzinémie [c18.452.132.100.380] Leighov syndróm [c18.452.132.100.412] Leschov-Nyhanov syndróm `[c18.452.132.100.425]` choroby lyzozómové, nervového systému [c18.452.132.100.435] + leucinóza [c18.452.132.100.520] MELAS syndróm [c18.452.132.100.535] Menkesov syndróm [c18.452.132.100.540] MERRF syndróm [c18.452.132.100.545] deficit mevalonátkinázy [c18.452.132.100.593] syndróm okulocerebrorenálny [c18.452.132.100.640] fenylketonúrie [c18.452.132.100.687] + choroba z deficitu pyruvátkarboxylázy [c18.452.132.100.725] choroba z deficitu pyruvátdehydrogenázového komplexu [c18.452.132.100.750] Refsumova choroba [c18.452.132.100.813] Refsumova choroba, infantilný typ [c18.452.132.100.844] tyrozinémie [c18.452.132.100.875] poruchy močovinového cyklu, vrodené [c18.452.132.100.937] + Zellwegerov syndróm [c18.452.132.100.968]
	`[c18.452.648.189.425]` choroby metabolické a poruchy výživy [c18] + choroby metabolické [c18.452] + poruchy metabolizmu, vrodené [c18.452.648] + choroby mozgu, metabolické vrodené [c18.452.648.189] + adrenoleukodystrofia [c18.452.648.189.084] angiopatia cerebrálna amyloidná familiárna [c18.452.648.189.168] galaktozémie [c18.452.648.189.320] Hartnupova choroba [c18.452.648.189.355] degenerácia hepatolentikulárna [c18.452.648.189.360] choroby centrálneho nervového systému demyelinizačné, dedičné [c18.452.648.189.362] + homocystinúria [c18.452.648.189.365] hyperglycinémia neketotická [c18.452.648.189.375] hyperlyzinémie [c18.452.648.189.380] Leighov syndróm [c18.452.648.189.412] Leschov-Nyhanov syndróm `[c18.452.648.189.425]` choroby lyzozómové, nervového systému [c18.452.648.189.435] + leucinóza [c18.452.648.189.520] MELAS syndróm [c18.452.648.189.535] Menkesov syndróm [c18.452.648.189.540] MERRF syndróm [c18.452.648.189.545] deficit mevalonátkinázy [c18.452.648.189.593] syndróm okulocerebrorenálny [c18.452.648.189.640] fenylketonúrie [c18.452.648.189.687] + choroba z deficitu pyruvátkarboxylázy [c18.452.648.189.725] choroba z deficitu pyruvátdehydrogenázového komplexu [c18.452.648.189.750] Refsumova choroba [c18.452.648.189.813] Refsumova choroba, infantilný typ [c18.452.648.189.844] tyrozinémie [c18.452.648.189.875] poruchy močovinového cyklu, vrodené [c18.452.648.189.937] + Zellwegerov syndróm [c18.452.648.189.968]
	`[c18.452.648.798.594]` choroby metabolické a poruchy výživy [c18] + choroby metabolické [c18.452] + poruchy metabolizmu, vrodené [c18.452.648] + poruchy metabolizmu purínu a pyrimidínu, vrodené [c18.452.648.798] + deficit dihydropyrimidíndehydrogenázy [c18.452.648.798.183] dna (choroba) [c18.452.648.798.368] + Leschov-Nyhanov syndróm `[c18.452.648.798.594]`

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Number of the records: 1

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