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
Q38336513-B1AC4E2D-F1D2-43F1-B643-6560E6D581D0
Q38336513-B1AC4E2D-F1D2-43F1-B643-6560E6D581D0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38336513-B1AC4E2D-F1D2-43F1-B643-6560E6D581D0
The congenital cranial dysinnervation disorders.
P2860
Q38336513-B1AC4E2D-F1D2-43F1-B643-6560E6D581D0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38336513-B1AC4E2D-F1D2-43F1-B643-6560E6D581D0
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
194d8bc0e6cf8721988da192d9077aadf3f297ef
P2860
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.