(Q1436162)
English
pantothenate kinase-associated neurodegeneration
A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13.
- Hallervorden-Spatz disease
- Hallervorden-Spatz syndrome
- brain Iron Accumulation type I syndrome
- neurodegeneration with brain iron accumulation 1
- NBIA1
- pigmentary pallidal degeneration (disorder)
- Pigmentary pallidal degeneration
- Neurodegeneration With Brain Iron Accumulation type 1
- Pantothenate Kinase-Associated Neurodegeneration
- NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1
- PKAN
- Pkan Neuroaxonal Dystrophy, Juvenile-Onset
Statements
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Pantothenate kinase-associated neurodegeneration
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Identifiers
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Sitelinks
Wikipedia(16 entries)
- arwiki تنكس عصبي مرتبط بكيناز البانتوثينات
- bswiki Pantotenat-kinazi pridruženi neurodegeneracijski protein
- cawiki Neurodegeneració associada a pantotenat-cinasa
- dewiki Pantothenatkinase-assoziierte Neurodegeneration
- elwiki Νόσος Χάλερβορντεν-Σπατς
- enwiki Pantothenate kinase-associated neurodegeneration
- eswiki Neurodegeneración asociada a pantotenato quinasa
- fiwiki PKAN-tauti
- frwiki Neurodégénerescence associée à la pantothénate kinase
- itwiki Neurodegenerazione associata alla pantotenato chinasi
- nlwiki Syndroom van Hallervorden-Spatz
- nowiki Pantotenate kinase-assosiert nevrodegenerativ sykdom
- plwiki Neurodegeneracja związana z kinazą pantotenianu
- ptwiki Neurodegeneração associada a pantotenato quinase
- ruwiki Болезнь Галлервордена — Шпатца
- simplewiki Pantothenate kinase-associated neurodegeneration