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1
Q37112108-b3ebd232-96f1-4183-a39c-9cfb5f15e1d2
Q37112108-b3ebd232-96f1-4183-a39c-9cfb5f15e1d2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37112108-b3ebd232-96f1-4183-a39c-9cfb5f15e1d2
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.
P31
Q37112108-b3ebd232-96f1-4183-a39c-9cfb5f15e1d2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37112108-b3ebd232-96f1-4183-a39c-9cfb5f15e1d2
rank
NormalRank
type
BestRank
Statement
P31
case report