wikimedia
/
wikidata
/
Login
Register
TriplyDB
Wikidata
Browser
Triples
Insights
Schema
BETA
Class frequency
Class hierarchy
SPARQL
Graphs
1
Q36273551-2185C698-5420-4A3F-9342-B11E6352DF16
Q36273551-2185C698-5420-4A3F-9342-B11E6352DF16
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36273551-2185C698-5420-4A3F-9342-B11E6352DF16
Point mutations in KAL1 and the mitochondrial gene MT-tRNA(cys) synergize to produce Kallmann syndrome phenotype.
P2860
Q36273551-2185C698-5420-4A3F-9342-B11E6352DF16
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36273551-2185C698-5420-4A3F-9342-B11E6352DF16
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
2cfcecfaae8206aaf4842426fdbde64bcc78c581
P2860
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness