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Q24533422-9586B4A6-452B-4209-A958-5DB8231BF44B
Q24533422-9586B4A6-452B-4209-A958-5DB8231BF44B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-9586B4A6-452B-4209-A958-5DB8231BF44B
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.
P2860
Q24533422-9586B4A6-452B-4209-A958-5DB8231BF44B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-9586B4A6-452B-4209-A958-5DB8231BF44B
rank
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type
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Statement
wasDerivedFrom
378e467c28c690041aa91f2577748182760a1f8e
P2860
Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43