| MSH |
D006211 |
C0018523 |
Hallervorden Spatz Syndrome |
preferred |
MSH |
D006211 |
C0018523 |
Hallervorden Spatz Disease |
no pref | MSH |
D006211 |
C0018523 |
HALLERVORDEN SPATZ DIS |
no pref | MSH |
D006211 |
C0018523 |
Neurodegeneration, Pantothenate Kinase-Associated |
no pref | MSH |
D006211 |
C0018523 |
Pantothenate Kinase Associated Neurodegeneration |
no pref | MSH |
D006211 |
C0018523 |
Pantothenate Kinase-Associated Neurodegeneration |
no pref | MSHCZE |
D006211 |
C0018523 |
Hallervordenův-Spatzův syndrom |
preferred | MSHPOR |
D006211 |
C0018523 |
Neurodegeneração Associada a Pantotenato-Quinase |
preferred | MSHSPA |
D006211 |
C0018523 |
Neurodegeneración Asociada a Pantotenato Quinasa |
no pref | MSHFIN |
D006211 |
C0018523 |
Pigmentoitunut pallidusrappeuma |
preferred | MSHFRE |
D006211 |
C0018523 |
Neurodégénérescence associée à la pantothénate kinase |
preferred | MSHGER |
D006211 |
C0018523 |
Pantothenat-Kinase-assoziierte Neurodegeneration |
preferred | MSHITA |
D006211 |
C0018523 |
Neurodegenerazione associata a pantotenato chinasi |
preferred | MSHRUS |
D006211 |
C0018523 |
PANTOTENATKINAZA-ASSOTSIIROVANNAIA NEIRODEGENERATSIIA |
no pref | MSHRUS |
D006211 |
C0018523 |
ХАЛЛЕРВОРДЕНА-ШПАТЦА СИНДРОМ |
no pref | MSHRUS |
D006211 |
C0018523 |
KHALLERVORDENA-SHPATTSA SINDROM |
no pref | MSHRUS |
D006211 |
C0018523 |
ПАНТОТЕНАТКИНАЗА-АССОЦИИРОВАННАЯ НЕЙРОДЕГЕНЕРАЦИЯ |
preferred | MSHRUS |
D006211 |
C0018523 |
DEGENERATSIIA BLEDNOGO SHARA PROGRESSIRUIUSHCHAIA |
no pref | MSH |
D006211 |
C0018523 |
Pallidal Atrophy, Pigmentary |
no pref | MSH |
D006211 |
C0018523 |
Degeneration, Pigmentary Pallidal |
no pref | MSHSWE |
D006211 |
C0018523 |
Pantotenatkinas-associerad neurodegeneration |
preferred | MSHPOL |
D006211 |
C0018523 |
Choroba Hallervordena-Spatza |
no pref | MSHPOL |
D006211 |
C0018523 |
Zwyrodnienie barwnikowe gałki bladej |
no pref | MSHPOL |
D006211 |
C0018523 |
Zwyrodnienie OUN związane z kinazą pantotenową |
preferred | MSHPOL |
D006211 |
C0018523 |
Zespół Hallervordena-Spatza |
no pref | MSHPOL |
D006211 |
C0018523 |
Neurodegeneracja związana z kinazą pantotenową |
no pref | MSH |
D006211 |
C0018523 |
PKAN Neuroaxonal Dystrophy, Juvenile Onset |
no pref | MSH |
D006211 |
C0018523 |
Juvenile-Onset Neuroaxonal Dystrophy |
no pref | MSH |
D006211 |
C0018523 |
Dystrophy, Juvenile-Onset Neuroaxonal |
no pref | MSH |
D006211 |
C0018523 |
Neuroaxonal Dystrophies, Juvenile-Onset |
no pref | MSH |
D006211 |
C0018523 |
Neuroaxonal Dystrophy, Juvenile Onset |
no pref | MSH |
D006211 |
C0018523 |
Dystrophies, Juvenile-Onset Neuroaxonal |
no pref | MSH |
D006211 |
C0018523 |
Juvenile-Onset Neuroaxonal Dystrophies |
no pref | MSHNOR |
D006211 |
C0018523 |
Pantotenat kinase-assosiert nevrodegenerativ sykdom |
preferred | MSHJPN |
D006211 |
C0018523 |
パントテン酸キナーゼ関連神経変性症 |
preferred | MSHJPN |
D006211 |
C0018523 |
神経変性症-パントテン酸キナーゼ関連 |
no pref | MSHJPN |
D006211 |
C0018523 |
神経変性疾患-パントテン酸キナーゼ関連 |
no pref | MSHJPN |
D006211 |
C0018523 |
Hallervorden-Spatz症候群 |
no pref | MSH |
D006211 |
C0018523 |
Hallervorden-Spatz Syndrome |
preferred | MSH |
D006211 |
C0018523 |
Pigmentary Pallidal Atrophy |
no pref | MSH |
D006211 |
C0018523 |
PKAN Neuroaxonal Dystrophy, Juvenile-Onset |
no pref | MSH |
D006211 |
C0018523 |
Neurodegeneration With Brain Iron Accumulation 1 |
no pref | MSH |
D006211 |
C0018523 |
Neuroaxonal Dystrophy, Juvenile-Onset |
no pref | MSH |
D006211 |
C0018523 |
Neurodegeneration with Brain Iron Accumulation Type 1 |
no pref | MSH |
D006211 |
C0018523 |
Pigmentary Pallidal Degeneration |
no pref | MSH |
D006211 |
C0018523 |
Hallervorden-Spatz Disease |
no pref | MSHITA |
D006211 |
C0018523 |
Sindrome di Hallervorden-Spatz |
no pref | MSHFRE |
D006211 |
C0018523 |
Dystrophie neuro-axonale tardive |
no pref | MSHITA |
D006211 |
C0018523 |
Atrofia pigmentaria del globo pallido |
no pref | MSHFRE |
D006211 |
C0018523 |
Maladie de Hallervorden-Spatz |
no pref | MSHGER |
D006211 |
C0018523 |
Globus-pallidus-Pigmentdegeneration |
no pref | MSHFRE |
D006211 |
C0018523 |
Neuroferritinopathie |
no pref | MSHSPA |
D006211 |
C0018523 |
Degeneración Palidal Pigmentaria |
no pref | MSHGER |
D006211 |
C0018523 |
Hallervorden-Spatz-Syndrom |
no pref | MSHGER |
D006211 |
C0018523 |
Pallidoretikuläre Pigmentdegeneration |
no pref | MSHCZE |
D006211 |
C0018523 |
Hallervordenova-Spatzova choroba |
no pref | MSHITA |
D006211 |
C0018523 |
Degenerazione pigmentaria del globo pallido |
no pref | MSHNOR |
D006211 |
C0018523 |
Hallervorden-Spatz' sykdom |
no pref | MSHNOR |
D006211 |
C0018523 |
Panthothenat kinase-assosiert nevrodegenerativ sykdom |
no pref | MSHCZE |
D006211 |
C0018523 |
neurodegenerace spojená s pantothenátkinasou |
no pref | MSHFRE |
D006211 |
C0018523 |
Neurodégénerescence avec accumulation de fer dans le cerveau |
no pref | MSHFRE |
D006211 |
C0018523 |
Dégénérescence pallidale pigmentaire |
no pref | MSHFRE |
D006211 |
C0018523 |
Syndrome de Hallervorden-Spatz |
no pref | MSHITA |
D006211 |
C0018523 |
Malattia di Hallervorden-Spatz |
no pref | MSHPOR |
D006211 |
C0018523 |
Degeneração Palidal Pigmentar |
no pref | MSHCZE |
D006211 |
C0018523 |
Hallervorden-Spatzova nemoc |
no pref | MSHFRE |
D006211 |
C0018523 |
Dystrophie neuroaxonale tardive |
no pref | MSHCZE |
D006211 |
C0018523 |
neuroaxonální degenerace s nástupem v mládí |
no pref | MSHSWE |
D006211 |
C0018523 |
Hallervorden-Spatz syndrom |
no pref | MSHJPN |
D006211 |
C0018523 |
ハラーホルデン・スパッツ症候群 |
no pref | MSHJPN |
D006211 |
C0018523 |
ハレルフォルデン-スパッツ症候群 |
no pref | MSHJPN |
D006211 |
C0018523 |
ハレルフォルデン・スパッツ症候群 |
no pref | MSHJPN |
D006211 |
C0018523 |
淡蒼球色素変性症 |
no pref | MSHJPN |
D006211 |
C0018523 |
Hallervorden-Spatz病 |
no pref | MSHJPN |
D006211 |
C0018523 |
ハレルフォルデン・シュパッツ病 |
no pref | MSHJPN |
D006211 |
C0018523 |
ハーラーフォルデン・スパッツ病 |
no pref | MSHRUS |
D006211 |
C0018523 |
ДЕГЕНЕРАЦИЯ БЛЕДНОГО ШАРА ПРОГРЕССИРУЮЩАЯ |
no pref | MSHDUT |
D006211 |
C0018523 |
Globus-pallidusdegeneratie |
no pref | MSHDUT |
D006211 |
C0018523 |
Hallervorden-Spatz-syndroom |
no pref | MSHDUT |
D006211 |
C0018523 |
Syndroom van Hallervorden-Spatz |
no pref | MSHDUT |
D006211 |
C0018523 |
Syndroom, Hallervorden-Spatz- |
preferred |