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Q42271720-CE2006CA-2593-4214-8BD0-DF5B6C32FBF5
Q42271720-CE2006CA-2593-4214-8BD0-DF5B6C32FBF5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42271720-CE2006CA-2593-4214-8BD0-DF5B6C32FBF5
Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entity.
P2860
Q42271720-CE2006CA-2593-4214-8BD0-DF5B6C32FBF5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42271720-CE2006CA-2593-4214-8BD0-DF5B6C32FBF5
rank
NormalRank
type
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Statement
wasDerivedFrom
bc4be211b00492efa58ea605c862f05e59e4c705
P2860
Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?