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References OMIM Gene GeneReviews HGMD HGNC
last update : 16/05/2008
Symbol HDL1
Location 20p13
Name Huntington-like 1
Other name(s) Huntington-like neurodegeneratice disorder 1
Corresponding gene PRNP
Other symbol(s) HLN1
Main clinical features
  • neurodegenerative disorder, prion disease, spongiform encephalopathy, early-onset with prominent psychiatric features, characterized by dementia, motor decline, and ataxia
  • Genetic determination autosomal dominant
    Related entries including prion disease with protracted course (in Brazilian people)
    Function/system disorder neurology
    psychiatric disorder
    Type disease
    Gene product
    Name prion protein