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Q24533422-AA5126FF-C53F-4D47-87ED-93E4AF0D8103
Q24533422-AA5126FF-C53F-4D47-87ED-93E4AF0D8103
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-AA5126FF-C53F-4D47-87ED-93E4AF0D8103
A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease.
P2860
Q24533422-AA5126FF-C53F-4D47-87ED-93E4AF0D8103
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24533422-AA5126FF-C53F-4D47-87ED-93E4AF0D8103
rank
NormalRank
type
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Statement
wasDerivedFrom
1aca124b02b3de9ff795b63fbd404d6b8359e465
P2860
Clinical manifestations of mitochondrial DNA depletion.