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Q34093285-357DC468-98CC-4985-8473-BF8ED8A1FD77
Q34093285-357DC468-98CC-4985-8473-BF8ED8A1FD77
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34093285-357DC468-98CC-4985-8473-BF8ED8A1FD77
A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.
P2860
Q34093285-357DC468-98CC-4985-8473-BF8ED8A1FD77
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34093285-357DC468-98CC-4985-8473-BF8ED8A1FD77
rank
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type
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Statement
wasDerivedFrom
1c008aaeca63e22dfc4b34aa5f64b4251ff66864
P2860
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.