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Q43500408-90425A05-0A95-4185-B7FF-DF041A7599F3
Q43500408-90425A05-0A95-4185-B7FF-DF041A7599F3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43500408-90425A05-0A95-4185-B7FF-DF041A7599F3
Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr-381 residue in FGFR2 gene.
P2860
Q43500408-90425A05-0A95-4185-B7FF-DF041A7599F3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43500408-90425A05-0A95-4185-B7FF-DF041A7599F3
rank
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type
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Statement
wasDerivedFrom
4d49f0521b66ed5171b698bdbf3fd2635fa670c6
P2860
Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling.