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Q48319168-7C5A0E78-B0C9-447C-B08A-72698C4A7F05
Q48319168-7C5A0E78-B0C9-447C-B08A-72698C4A7F05
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48319168-7C5A0E78-B0C9-447C-B08A-72698C4A7F05
A 10q21.3q22.2 microdeletion identified in a patient with severe developmental delay and multiple congenital anomalies including congenital heart defects.
P2860
Q48319168-7C5A0E78-B0C9-447C-B08A-72698C4A7F05
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48319168-7C5A0E78-B0C9-447C-B08A-72698C4A7F05
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7e5a3fbf0eee78a75ae76861bcc16753756910f9
P2860
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder