awgldk
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q42538852-4E571578-1DD3-4C86-9E9D-684E5922130B
Q42538852-4E571578-1DD3-4C86-9E9D-684E5922130B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-4E571578-1DD3-4C86-9E9D-684E5922130B
'Behr syndrome' with OPA1 compound heterozygote mutations.
P2860
Q42538852-4E571578-1DD3-4C86-9E9D-684E5922130B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42538852-4E571578-1DD3-4C86-9E9D-684E5922130B
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
54d0087ae6b30278899a272aa58f1532fe8cc966
P2860
Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews