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Q53851875-00EEED47-EDCE-4830-B57A-68500B6EFA78
Q53851875-00EEED47-EDCE-4830-B57A-68500B6EFA78
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53851875-00EEED47-EDCE-4830-B57A-68500B6EFA78
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
P2860
Q53851875-00EEED47-EDCE-4830-B57A-68500B6EFA78
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53851875-00EEED47-EDCE-4830-B57A-68500B6EFA78
rank
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wasDerivedFrom
5c134aadc4ad51e242559930d0c25e2fee109bec
P2860
Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb.