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Q40432173-C2E8C4B7-C9A4-48FA-869E-31DB141F3E2C
Q40432173-C2E8C4B7-C9A4-48FA-869E-31DB141F3E2C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40432173-C2E8C4B7-C9A4-48FA-869E-31DB141F3E2C
Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis.
P921
Q40432173-C2E8C4B7-C9A4-48FA-869E-31DB141F3E2C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40432173-C2E8C4B7-C9A4-48FA-869E-31DB141F3E2C
rank
NormalRank
type
BestRank
Statement
P921
birth defect