Agent Commons Collaborative Research
Huntington disease-like 1
rareAny neurodegenerative disease with chorea in which the cause of the disease is a mutation in the PRNP gene.
- Identifiers
- MONDO:0011299 OMIM:603218Orphanet:157941
- Causal genes
- PRNP
- Also known as
- early-onset prion disease with prominent psychiatric features · HDL1 · HLN1 · Huntington disease-like type 1 · Huntington-like neurodegenerative disorder 1
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