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Multiple congenital anomaly caused by deletion on chromosome 11

Property Value
dbo:description
  • حالة طبية (ar)
  • rara malattia congenita (it)
  • Genetik hastalık (tr)
  • autosomal vererbte Erkrankung (de)
  • multiple congenital anomaly caused by deletion on chromosome 11 (en)
dbo:diseasesDB
  • 31957
dbo:icd10
  • Q93.5
dbo:icd9
  • 758.3
dbo:omim
  • 147791 (xsd:integer)
dbo:thumbnail
dbo:wikiPageWikiLink
dbp:caption
  • A girl displaying characteristic facial features of Jacobsen syndrome (en)
dbp:diseasesdb
  • 31957 (xsd:integer)
dbp:icd
  • 758.300000 (xsd:double)
  • Q93.5 (en)
dbp:name
  • Jacobsen syndrome (en)
dbp:omim
  • 147791 (xsd:integer)
dbp:synonyms
  • Del, distal deletion 11q, distal monosomy 11q, monosomy 11qter (en)
dbp:wikiPageUsesTemplate
dbp:wordnet_type
dct:subject
rdf:type
rdfs:label
  • Jacobsen syndrome (en)
  • متلازمة جاكوبسن (ar)
  • Jacobsen-Syndrom (de)
  • Σύνδρομο Γιάκομπσεν (el)
  • Síndrome de Jacobsen (es)
  • Sindrome di Jacobsen (it)
  • Syndrome de Jacobsen (fr)
  • Syndroom van Jacobsen (nl)
  • Zespół Jacobsen (pl)
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