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Q26852658-ED392F08-DE01-4D1B-A687-290F056F73AD
Q26852658-ED392F08-DE01-4D1B-A687-290F056F73AD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26852658-ED392F08-DE01-4D1B-A687-290F056F73AD
Cystinuria: an inborn cause of urolithiasis
P2860
Q26852658-ED392F08-DE01-4D1B-A687-290F056F73AD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26852658-ED392F08-DE01-4D1B-A687-290F056F73AD
rank
NormalRank
type
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Statement
wasDerivedFrom
a7f3c55a0ff49ef31c83da24c22b2d91b740a6bc
P2860
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.