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

Glutaminase deficiency is a rare genetic disorder that presents in childhood. It is associated with epilepsy and usually results in an early demise.

Property Value
dbo:abstract
  • Glutaminase deficiency is a rare genetic disorder that presents in childhood. It is associated with epilepsy and usually results in an early demise. (en)
dbo:thumbnail
dbo:wikiPageID
  • 60471105 (xsd:integer)
dbo:wikiPageLength
  • 2832 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID
  • 992166248 (xsd:integer)
dbo:wikiPageWikiLink
dbp:caption
  • Glutaminase deficiency is inherited via an autosomal recessive manner (en)
dbp:causes
  • Mutation in GLS gene (en)
dbp:name
  • Glutaminase deficiency (en)
dbp:wikiPageUsesTemplate
dct:subject
rdf:type
rdfs:comment
  • Glutaminase deficiency is a rare genetic disorder that presents in childhood. It is associated with epilepsy and usually results in an early demise. (en)
rdfs:label
  • Glutaminase deficiency (en)
owl:sameAs
prov:wasDerivedFrom
foaf:depiction
foaf:isPrimaryTopicOf
foaf:name
  • Glutaminase deficiency (en)
is foaf:primaryTopic of
Powered by OpenLink Virtuoso    This material is Open Knowledge     W3C Semantic Web Technology     This material is Open Knowledge    Valid XHTML + RDFa
This content was extracted from Wikipedia and is licensed under the Creative Commons Attribution-ShareAlike 3.0 Unported License
  NODES
Note 1