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
Q37741094-2FAFA201-2E85-452A-A644-CE744A466C7D
Q37741094-2FAFA201-2E85-452A-A644-CE744A466C7D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37741094-2FAFA201-2E85-452A-A644-CE744A466C7D
Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation.
P2860
Q37741094-2FAFA201-2E85-452A-A644-CE744A466C7D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37741094-2FAFA201-2E85-452A-A644-CE744A466C7D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
34a1df22ce1c29be8e9b9ca2d4f44b8f498842e1
P2860
Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis.