JSON

autosomal recessive spastic paraplegia type 66

^ http://purl.obolibrary.org/obo/MONDO_0018418

Term info

database cross reference
  • Orphanet:401815 (MONDO:equivalentTo)
  • UMLS:CN226125 (MONDO:equivalentTo)
Subsets

ordo_disease

abbreviation
SPG66 [ Orphanet:401815 ]

exactMatch

http://purl.obolibrary.org/obo/Orphanet_401815, http://linkedlifedata.com/resource/umls/id/CN226125

id

MONDO:0018418