Term info
database cross reference
- UMLS:CN226593 (MONDO:equivalentTo)
- Orphanet:100979 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
Autosomal dominant form of complex hereditary spastic paraplegia.
exactMatch
http://linkedlifedata.com/resource/umls/id/CN226593, http://purl.obolibrary.org/obo/Orphanet_100979
has exact synonym
autosomal dominant complicated spastic paraplegia, autosomal dominant complicated HSP, autosomal dominant complicated SPG, complex hereditary spastic paraplegia, autosomal dominant, autosomal dominant complex hereditary spastic paraplegia, autosomal dominant complex SPG, autosomal dominant complex HSP
id
MONDO:0015087