About: Weyer's ulnar ray/oligodactyly syndrome

An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Weyer's ulnar ray/oligodactyly syndrome is a rare multi-systemic genetic disorder which is characterized by ectrodactyly, ulnar, radial, or fibular ray deficit, and heart, single central incisor, splenic, and renal abnormalities. Cleft lip/palate and hypoplasia of the mandibles have also been observed. It is thought to be inherited in an autosomal recessive pattern. It was first discovered in 1957 by Weyers et al. Only four families worldwide are known to be affected by the disorder.

Property	Value
dbo:abstract	Weyer's ulnar ray/oligodactyly syndrome is a rare multi-systemic genetic disorder which is characterized by ectrodactyly, ulnar, radial, or fibular ray deficit, and heart, single central incisor, splenic, and renal abnormalities. Cleft lip/palate and hypoplasia of the mandibles have also been observed. It is thought to be inherited in an autosomal recessive pattern. It was first discovered in 1957 by Weyers et al. Only four families worldwide are known to be affected by the disorder. (en)
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dbo:wikiPageRevisionID	1099035818 (xsd:integer)
dbo:wikiPageWikiLink	dbr:Death dbc:Rare_genetic_syndromes dbr:Genetic_disorder dbr:Genetic_mutation dbr:Medical_genetics dbr:Ulnar_dysplasia
dbp:causes	dbr:Genetic_mutation
dbp:complications	Possible death (en)
dbp:deaths	- (en)
dbp:duration	Life-long (en)
dbp:frequency	Very rare. only 4 families known to carry the gene/be affected by the gene (en)
dbp:name	Weyer's ulnar ray/oligodactyly syndrome (en)
dbp:onset	Birth (en)
dbp:prevention	None (en)
dbp:prognosis	Ok (en)
dbp:specialty	dbr:Medical_genetics
dbp:symptoms	Ulnar ray deficit, heart, renal and splenic abnormalities and ectrodactyly (en)
dbp:wikiPageUsesTemplate	dbt:Reflist dbt:Infobox_medical_condition
dcterms:subject	dbc:Rare_genetic_syndromes
rdf:type	owl:Thing wikidata:Q12136 dbo:Disease
rdfs:comment	Weyer's ulnar ray/oligodactyly syndrome is a rare multi-systemic genetic disorder which is characterized by ectrodactyly, ulnar, radial, or fibular ray deficit, and heart, single central incisor, splenic, and renal abnormalities. Cleft lip/palate and hypoplasia of the mandibles have also been observed. It is thought to be inherited in an autosomal recessive pattern. It was first discovered in 1957 by Weyers et al. Only four families worldwide are known to be affected by the disorder. (en)
rdfs:label	Weyer's ulnar ray/oligodactyly syndrome (en)
owl:sameAs	wikidata:Weyer's ulnar ray/oligodactyly syndrome https://global.dbpedia.org/id/E4CiV
prov:wasDerivedFrom	wikipedia-en:Weyer's_ulnar_ray/oligodactyly_syndrome?oldid=1099035818&ns=0
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