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Q36983068-572B8AD7-F4D9-42D7-B26D-2DEE00DA7275
Q36983068-572B8AD7-F4D9-42D7-B26D-2DEE00DA7275
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36983068-572B8AD7-F4D9-42D7-B26D-2DEE00DA7275
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations
P921
Q36983068-572B8AD7-F4D9-42D7-B26D-2DEE00DA7275
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36983068-572B8AD7-F4D9-42D7-B26D-2DEE00DA7275
rank
NormalRank
type
BestRank
Statement
P921
osteogenesis imperfecta