pantothenate kinase-associated neurodegeneration (Q1436162)
neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13
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aliases 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
description neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13

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(P11143) Pantothenate kinase-associated neurodegeneration
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