MeSH Browser

MeSH Supplementary: Huntington Disease-Like 1
Unique ID: C566398
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566398
Entry Term(s): Huntington-Like Neurodegenerative Disorder 1; Huntington-Like Neurodegenerative Disorder, Autosomal Dominant; Prion Disease, Early-Onset, With Prominent Psychiatric Features
Heading Mapped to: *Huntington Disease
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Huntington Disease-Like 1 MeSH Supplementary Concept Data 2024