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Q24533422-1C584062-A761-43BA-86A0-60E27B49662B
Q24533422-1C584062-A761-43BA-86A0-60E27B49662B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-1C584062-A761-43BA-86A0-60E27B49662B
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.
P2860
Q24533422-1C584062-A761-43BA-86A0-60E27B49662B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-1C584062-A761-43BA-86A0-60E27B49662B
rank
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type
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Statement
wasDerivedFrom
378e467c28c690041aa91f2577748182760a1f8e
P2860
Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine