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1
Q37112108-14FA4DA1-C6B7-4812-BACF-1500331055E2
Q37112108-14FA4DA1-C6B7-4812-BACF-1500331055E2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37112108-14FA4DA1-C6B7-4812-BACF-1500331055E2
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.
P2860
Q37112108-14FA4DA1-C6B7-4812-BACF-1500331055E2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37112108-14FA4DA1-C6B7-4812-BACF-1500331055E2
rank
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type
BestRank
Statement
wasDerivedFrom
d507fb356dddf410f495f3744f59073e776d5314
P2860
A family with optic atrophy and congenital hearing loss.