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Q24324233-C87800D4-D0BA-45D4-B186-415CEFD0E09D
Q24324233-C87800D4-D0BA-45D4-B186-415CEFD0E09D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24324233-C87800D4-D0BA-45D4-B186-415CEFD0E09D
Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene
P2860
Q24324233-C87800D4-D0BA-45D4-B186-415CEFD0E09D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24324233-C87800D4-D0BA-45D4-B186-415CEFD0E09D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
1e32d8328e461371c308145f06ded1abd4030abe
P2860
Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1A.