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

The 49,XXXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of three extra X chromosomes in males

Property Value
dbo:description
  • Kelainan kromosom jenis aneuploidi dengan tiga kromosom X tambahan pada laki-laki (in)
  • The 49,XXXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of three extra X chromosomes in males (en)
dbo:diseasesDB
  • 32552
dbo:gradName
  • 49,XXXXY syndrome
dbo:gradNum
  • 5679
dbo:icd10
  • Q98.1
dbo:icd9
  • 758.7
dbo:medicalCause
dbo:medicalDiagnosis
dbo:medicalSpecialty
dbo:meshId
  • D007713
dbo:orpha
  • 96264
dbo:synonym
  • 49,XXXXY syndrome
  • Fraccaro syndrome
dbo:thumbnail
dbo:wikiPageExternalLink
dbo:wikiPageWikiLink
dbp:caption
  • A 19-year-old man with XXXXY syndrome and prognathism (en)
dbp:causes
  • Cellular nondisjunction during meiosis (en)
dbp:diagnosis
dbp:diseasesdb
  • 32552 (xsd:integer)
dbp:duration
  • Lifelong (en)
dbp:frequency
  • 1 (xsd:integer)
dbp:gardname
  • 49 (xsd:integer)
dbp:gardnum
  • 5679 (xsd:integer)
dbp:icd
  • 758.700000 (xsd:double)
  • (en)
  • Q98.1 (en)
dbp:meshid
  • D007713 (en)
dbp:name
  • XXXXY syndrome (en)
dbp:onset
  • Prenatal (en)
dbp:orphanet
  • 96264 (xsd:integer)
dbp:scholia
  • Q4638720 (en)
dbp:snomedCt
  • 38847009 (xsd:integer)
dbp:specialty
dbp:synonym
  • Fraccaro syndrome 49,XXXXY syndrome (en)
dbp:wikiPageUsesTemplate
dct:subject
rdf:type
rdfs:label
  • XXXXY syndrome (en)
  • Sindrom 49, XXXXY (in)
  • XXXXY 증후군 (ko)
  • Síndrome XXXXY (pt)
  • Синдром 49, XXXXY (ru)
  • XXXXY综合征 (zh)
owl:sameAs
prov:wasDerivedFrom
foaf:depiction
foaf:isPrimaryTopicOf
foaf:name
  • XXXXY syndrome (en)
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