JSON

autosomal recessive spastic paraplegia type 69

^ http://purl.obolibrary.org/obo/MONDO_0018421

Term info

database cross reference
  • UMLS:CN226128 (MONDO:equivalentTo)
  • Orphanet:401830 (MONDO:equivalentTo)
Subsets

ordo_disease

abbreviation
SPG69 [ Orphanet:401830 ]

exactMatch

http://purl.obolibrary.org/obo/Orphanet_401830, http://linkedlifedata.com/resource/umls/id/CN226128

id

MONDO:0018421