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Rare genetic condition in humans

Property Value
dbo:description
  • malattia genetica legata al cromosoma X (it)
  • rare genetic condition in humans (en)
dbo:diseasesDB
  • 32654
dbo:geneReviewsId
  • NBK1676
dbo:geneReviewsName
  • MED12-Related Disorders (en)
dbo:icd10
  • F70.1
dbo:icd9
  • 317
dbo:medicalSpecialty
dbo:omim
  • 309520 (xsd:integer)
dbo:thumbnail
dbo:wikiPageExternalLink
dbo:wikiPageWikiLink
dbp:caption
  • Lujan–Fryns syndrome in a young adult male, with features that include a long, narrow face and recessed chin. (en)
dbp:imageSize
  • 300 (xsd:integer)
dbp:name
  • Lujan–Fryns syndrome (en)
dbp:specialty
dbp:synonyms
  • X-linked mental retardation with Marfanoid habitus, Lujan syndrome (en)
dbp:wikiPageUsesTemplate
dct:subject
gold:hypernym
rdf:type
rdfs:label
  • Lujan–Fryns syndrome (en)
  • متلازمة لوجان-فرينس (ar)
  • Lujan-Fryns-Syndrom (de)
  • Syndrome de Lujan-Fryns (fr)
  • Sindrome di Lujan-Fryns (it)
  • Zespół Lujana-Frynsa (pl)
owl:sameAs
prov:wasDerivedFrom
foaf:depiction
foaf:isPrimaryTopicOf
foaf:name
  • Lujan–Fryns syndrome (en)
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