Mietens syndrome (original) (raw)

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dbo:abstract Mietens syndrome is a autosomal recessive disorder first described by Mietens and Weber. The condition is named after a German physician named Carl Mietens. Only 9 cases have been reported. (en)
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dbo:wikiPageWikiLink dbr:Sclerocornea dbr:Nystagmus dbc:Autosomal_recessive_disorders dbr:Strabismus dbr:Autosomal_recessive dbr:Flat_feet dbr:Intellectual_disability dbr:Severe_postnatal_growth_retardation dbr:Short_forearm_bones
dbp:caption This condition is inherited via an autosomal recessive pattern (en)
dbp:name Mietens syndrome (en)
dbp:synonym *Intellectual disability, Mietens-Weber type * Mietens-Weber syndrome * Corneal opacity, nystagmus, flexion contracture of the elbows, growth failure, and mental retardation * Mental retardation syndrome, Mietens Weber type (en)
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dcterms:subject dbc:Autosomal_recessive_disorders
rdf:type owl:Thing wikidata:Q12136 dbo:Disease
rdfs:comment Mietens syndrome is a autosomal recessive disorder first described by Mietens and Weber. The condition is named after a German physician named Carl Mietens. Only 9 cases have been reported. (en)
rdfs:label Mietens syndrome (en)
owl:sameAs wikidata:Mietens syndrome https://global.dbpedia.org/id/E7nAd
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