Kufor-Rakeb syndrome (Q6441908)

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Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment
  • PARK9
  • autosomal recessive Parkinson disease 9
  • autosomal recessive juvenile onset Parkinson disease 9
  • Parkinson Disease 9, Autosomal Recessive
  • Ceroid Lipofuscinosis, Neuronal, 12
  • KUFOR-RAKEB SYNDROME; KRS
  • KUFOR-RAKEB SYNDROME
  • Pallidopyramidal Degeneration With Supranuclear Upgaze Paresis and Dementia
  • KRS
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English
Kufor-Rakeb syndrome
Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment
  • PARK9
  • autosomal recessive Parkinson disease 9
  • autosomal recessive juvenile onset Parkinson disease 9
  • Parkinson Disease 9, Autosomal Recessive
  • Ceroid Lipofuscinosis, Neuronal, 12
  • KUFOR-RAKEB SYNDROME; KRS
  • KUFOR-RAKEB SYNDROME
  • Pallidopyramidal Degeneration With Supranuclear Upgaze Paresis and Dementia
  • KRS

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C203534
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