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Huntington disease-like 1

Disease Summary
Associated Targets (2)
Tchem

1

Tbio

1


Mondo Description Any neurodegenerative disease with chorea in which the cause of the disease is a mutation in the PRNP gene.
Uniprot Description Autosomal dominant, early-onset neurodegenerative disorder with prominent psychiatric features.
Mondo Term and Equivalent IDs
MONDO:0011299:  Huntington disease-like 1
MESH:C566398: 
Orphanet:157941: 
UMLS:C1864112: