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) |
dbo:thumbnail |
wiki-commons:Special:FilePath/Autosomal_recessive_-_en.svg?width=300 |
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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) |
dbp:wikiPageUsesTemplate |
dbt:Lead_too_short dbt:Reflist dbt:Infobox_medical_condition |
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 |
prov:wasDerivedFrom |
wikipedia-en:Mietens_syndrome?oldid=1051139686&ns=0 |
foaf:depiction |
wiki-commons:Special:FilePath/Autosomal_recessive_-_en.svg |
foaf:isPrimaryTopicOf |
wikipedia-en:Mietens_syndrome |
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dbr:List_of_diseases_(M) |
is foaf:primaryTopic of |
wikipedia-en:Mietens_syndrome |