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Q24311734-01933587-41B2-4586-9B6A-885F53C77073
Q24311734-01933587-41B2-4586-9B6A-885F53C77073
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24311734-01933587-41B2-4586-9B6A-885F53C77073
Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition
P2860
Q24311734-01933587-41B2-4586-9B6A-885F53C77073
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24311734-01933587-41B2-4586-9B6A-885F53C77073
rank
NormalRank
type
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Statement
wasDerivedFrom
4fee7f251d91b318608af75467bc45d8f1981a98
P2860
A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.