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Q39038032-1B85AFC9-E106-4A80-B36C-29DC9E21B373
Q39038032-1B85AFC9-E106-4A80-B36C-29DC9E21B373
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39038032-1B85AFC9-E106-4A80-B36C-29DC9E21B373
Complicated hereditary spastic paraparesis with cerebral white matter lesions.
P2860
Q39038032-1B85AFC9-E106-4A80-B36C-29DC9E21B373
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39038032-1B85AFC9-E106-4A80-B36C-29DC9E21B373
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
9fbf445e6a7da9902e94765af63989f7ffc5c469
P2860
A familial syndrome of infantile optic atrophy, movement disorder, and spastic paraplegia.