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Q24533422-012084CE-1720-4603-8C51-BB3E3444ACE2
Q24533422-012084CE-1720-4603-8C51-BB3E3444ACE2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-012084CE-1720-4603-8C51-BB3E3444ACE2
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.
P2860
Q24533422-012084CE-1720-4603-8C51-BB3E3444ACE2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-012084CE-1720-4603-8C51-BB3E3444ACE2
rank
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type
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wasDerivedFrom
7b58157747859b308c6995fe688aa24475c66bbf
P2860
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.