Huntington disease-like syndrome due to C9ORF72 expansions
http://purl.obolibrary.org/obo/MONDO_0018425
Term info
database cross reference
- Orphanet:401901 (MONDO:equivalentTo)
- UMLS:CN226138 (MONDO:equivalentTo)
Subsets
ordo_disease
exactMatch
http://linkedlifedata.com/resource/umls/id/CN226138, http://purl.obolibrary.org/obo/Orphanet_401901
has exact synonym
C9ORF72-related Huntington disease-like syndrome, C9ORF72-related Huntington disease phenocopy, Huntington disease phenocopy due to C9ORF72 expansions
id
MONDO:0018425
Term relations
Subclass of:
- movement disorder
- Huntington disease-like syndrome
- has characteristic some rare
- disease has major feature some dementia