wikimedia
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Table
SPARQL
Graphs
1
1
Services
1
1
Assets
0
0
Insights
Schema
BETA
Class frequency
Class hierarchy
Q33406025-AD6349DF-7685-4142-81CF-54AF8D90371D
Q33406025-AD6349DF-7685-4142-81CF-54AF8D90371D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33406025-AD6349DF-7685-4142-81CF-54AF8D90371D
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.
P2860
Q33406025-AD6349DF-7685-4142-81CF-54AF8D90371D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33406025-AD6349DF-7685-4142-81CF-54AF8D90371D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
19deb3c3d44f6dd184a8e60dc5bbe6667898df0f
P2860
The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.