<nowiki>sindrome di Hallervorden-Spatz; neurodégénerescence associée à la pantothénate kinase; Болезнь Галлервордена—Шпатца; Neurodegeneration mit Eisenablagerung im Gehirn; neurodegeneração associada a pantotenato quinase; Pantothenate kinase-associated neurodegeneration; 泛酸鹽激活酵素關聯之神經退化性疾病; パントテン酸キナーゼ関連神経変性症; Neurodegeneração associada a pantotenato quinase; neurodegeneración asociada a pantotenato quinasa; 泛酸鹽激活酵素關聯之神經退化性疾病; Choroba Hallervordena-Spatza; Pantotenate kinase-assosiert nevrodegenerativ sykdom; syndroom van Hallervorden-Spatz; 泛酸鹽啟用酵素關聯之神經退化性疾病; تنكس عصبي مرتبط بكيناز البانتوثينات; neurodegeneració associada a pantotenat-cinasa; PKAN-tauti; pantothenate kinase-associated neurodegeneration; Pantothenate kinase-associated neurodegeneration; Νόσος Χάλερβορντεν-Σπατς; Pantotenat-kinazi pridruženi neurodegeneracijski protein; malattia autosomica recessiva, legata al cromosoma 20,caratterizzata da degenerazione cerebrale; Krankheit; Doença genética neurodegenerativa com acumulação de ferro no cérebro; A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13.; хвороба; dégénérescence cérébrale par accumulation de fer dans les noyaux gris centraux; neurodegenerazione con accumulo di ferro; neurodegenerazione con accumulo di ferro a livello cerebrale; 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; νευροεκφυλισμός που σχετίζεται με την παντοθενική κινάση; Neurodegeneracion asociada a pantotenato quinasa</nowiki>
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.
