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Q42538852-7E57FAB9-5263-4A63-972E-847354E47972
Q42538852-7E57FAB9-5263-4A63-972E-847354E47972
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-7E57FAB9-5263-4A63-972E-847354E47972
'Behr syndrome' with OPA1 compound heterozygote mutations.
P2860
Q42538852-7E57FAB9-5263-4A63-972E-847354E47972
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-7E57FAB9-5263-4A63-972E-847354E47972
rank
NormalRank
type
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Statement
wasDerivedFrom
54d0087ae6b30278899a272aa58f1532fe8cc966
P2860
A familial syndrome of infantile optic atrophy, movement disorder, and spastic paraplegia.