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
Q35869509-9A245E19-4D0D-4DE3-A3F5-267181A8A7E8
Q35869509-9A245E19-4D0D-4DE3-A3F5-267181A8A7E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35869509-9A245E19-4D0D-4DE3-A3F5-267181A8A7E8
Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.
P2860
Q35869509-9A245E19-4D0D-4DE3-A3F5-267181A8A7E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35869509-9A245E19-4D0D-4DE3-A3F5-267181A8A7E8
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
06d73df2fa64eb79efa6189562feb8443daa8f73
P2860
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome