| dbo:description
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- genetic disease (en)
- choroba uwarunkowana genetycznie (pl)
- Angeborene Erkrankung der Bauchspeicheldrüse (de)
- maladie génétique se manifestant par une hypoglycémie (fr)
- הפרעה מולדת (iw)
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| dbo:eMedicineSubject
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| dbo:eMedicineTopic
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| dbo:icd9
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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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| dbp:causes
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- ABCC8 gene mutations (en)
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| dbp:diagnosis
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| dbp:emedicinesubj
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| dbp:emedicinetopic
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| dbp:icd
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- 251.100000 (xsd:double)
- (en)
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| dbp:meshid
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| dbp:name
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- Congenital hyperinsulinism (en)
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| dbp:omim
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| dbp:symptoms
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| dbp:synonyms
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- CHI, familial hyperinsulinism, hyperinsulinemic hypoglycemia of infancy (en)
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| dbp:treatment
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- Diazoxide, octreotide (en)
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| dbp:wikiPageUsesTemplate
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| dct:subject
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| gold:hypernym
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| rdf:type
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| rdfs:label
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- Congenital hyperinsulinism (en)
- فرط الأنسولينية الخلقي (ar)
- Kongenitaler Hyperinsulinismus (de)
- Hyperinsulinisme familial (fr)
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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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- Congenital hyperinsulinism (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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