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Q51158820-0ED14F06-CB3B-4906-8A71-07EE7745A1D5
Q51158820-0ED14F06-CB3B-4906-8A71-07EE7745A1D5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-0ED14F06-CB3B-4906-8A71-07EE7745A1D5
Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies.
P2860
Q51158820-0ED14F06-CB3B-4906-8A71-07EE7745A1D5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51158820-0ED14F06-CB3B-4906-8A71-07EE7745A1D5
rank
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type
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Statement
wasDerivedFrom
33180124bff4e3ca3d54bcb0c98fdfbfea34aa9c
P2860
Spondylocarpotarsal synostosis with hydromyelia, mega cisterna magna, and pachydermoperiostosis.