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Q37112108-F45EDBEF-5282-4110-98B0-3551F84051BB
Q37112108-F45EDBEF-5282-4110-98B0-3551F84051BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37112108-F45EDBEF-5282-4110-98B0-3551F84051BB
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.
P2860
Q37112108-F45EDBEF-5282-4110-98B0-3551F84051BB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37112108-F45EDBEF-5282-4110-98B0-3551F84051BB
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wasDerivedFrom
de73d920ea81061f5e99f53ab3633b10ced822ac
P2860
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus.