About: Ornithine translocase deficiency

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

Amino acid metabolic disorder that has material basis in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood

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dbo:description
  • maladie (fr)
  • Krankheit (de)
  • хвороба (uk)
  • amino acid metabolic disorder that has material basis in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood (en)
dbo:diseasesDB
  • 29849
dbo:icd9
  • 270.6
dbo:omim
  • 238970 (xsd:integer)
dbo:orpha
  • 415
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dbo:wikiPageExternalLink
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dbp:diseasesdb
  • 29849 (xsd:integer)
dbp:icd
  • 270.600000 (xsd:double)
  • (en)
dbp:name
  • Ornithine translocase deficiency (en)
dbp:omim
  • 238970 (xsd:integer)
dbp:orphanet
  • 415 (xsd:integer)
dbp:synonyms
  • HHH syndrome, ORNT1 deficiency, ornithine carrier deficiency, triple H syndrome (en)
dbp:wikiPageUsesTemplate
dbp:wordnet_type
dct:subject
gold:hypernym
rdf:type
rdfs:label
  • Ornithine translocase deficiency (en)
  • HHH-Syndrom (de)
  • 高鳥胺酸血症-高氨血症-高瓜胺酸血症候群 (zh)
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foaf:depiction
foaf:isPrimaryTopicOf
foaf:name
  • Ornithine translocase deficiency (en)
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