pantothenate kinase-associated neurodegeneration (Q1436162)

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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
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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

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Pantothenate kinase-associated neurodegeneration
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