| dbo:description
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- Krankheit (de)
- malattia (it)
- хвороба (uk)
- missbildning av ansiktets skelett- och muskeluppbyggnad (sv)
- ou Séquence de Pierre Robin (SPR) (fr)
- prirojeno stanje z mikrognatijo in glosoptozo (sl)
- врождённый порок (ru)
- a congenital condition with micrognathia and glossoptosis (en)
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| dbo:diseasesDB
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| dbo:eMedicineSubject
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| dbo:eMedicineTopic
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| dbo:icd10
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| dbo:icd9
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| dbo:medicalCause
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| dbo:medicalDiagnosis
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| dbo:medlinePlus
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| dbo:meshId
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| dbo:omim
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| dbo:symptom
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| dbo:thumbnail
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| dbo:treatment
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| dbo:wikiPageExternalLink
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| dbo:wikiPageWikiLink
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| dbp:caption
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- Infant with Pierre Robin sequence (en)
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| dbp:causes
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- intrauterine compression of fetal mandible, de-novo mutations or Stickler syndrome (en)
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| dbp:diagnosis
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| dbp:diseasesdb
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| dbp:emedicinesubj
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| dbp:emedicinetopic
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| dbp:field
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| dbp:frequency
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| dbp:icd
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- 756 (xsd:integer)
- (en)
- Q87.0 (en)
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| dbp:medlineplus
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| dbp:meshid
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| dbp:name
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- Pierre Robin sequence (en)
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| dbp:omim
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| dbp:onset
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- During gestation, present at birth (en)
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| dbp:symptoms
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- Micrognathia, glossoptosis, obstruction of the upper airway, sometimes cleft palate (en)
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| dbp:synonyms
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- Pierre Robin syndrome, Pierre Robin malformation, Pierre Robin anomaly, Pierre Robin anomalad (en)
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| dbp:treatment
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| dbp:wikiPageUsesTemplate
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| dct:subject
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| rdf:type
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| rdfs:label
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- Pierre Robin sequence (en)
- متلازمة بيير روبين (ar)
- Pierre-Robin-Sequenz (de)
- Robinen sindromea (eu)
- Síndrome de Pierre Robin (es)
- Syndrome de Pierre Robin (fr)
- Sindrome di Pierre Robin (it)
- Síndrome de Pierre Robin (pt)
- Syndroom van Pierre Robin (nl)
- Zespół Pierre’a Robina (pl)
- Pierre Robins sekvens (sv)
- Синдром Робена (ru)
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| owl:sameAs
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| prov:wasDerivedFrom
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| foaf:depiction
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| foaf:isPrimaryTopicOf
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| foaf:name
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- Pierre Robin sequence (en)
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| is dbo:wikiPageRedirects
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| is dbo:wikiPageWikiLink
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| is foaf:primaryTopic
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