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Q38241672-60B66126-4BD3-47F8-B057-EF00D9FD0351
Q38241672-60B66126-4BD3-47F8-B057-EF00D9FD0351
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38241672-60B66126-4BD3-47F8-B057-EF00D9FD0351
Human genetic disorders of sphingolipid biosynthesis.
P2860
Q38241672-60B66126-4BD3-47F8-B057-EF00D9FD0351
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38241672-60B66126-4BD3-47F8-B057-EF00D9FD0351
rank
NormalRank
type
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Statement
wasDerivedFrom
723fc4ef881f3b1302017f490043ec4e51a728e6
P2860
Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis.