| dbo:description
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- Krankheit (de)
- хвороба (uk)
- مرض يصيب الإنسان (ar)
- glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity (en)
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| dbo:geneReviewsId
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| dbo:geneReviewsName
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- Phosphorylase Kinase Deficiency (en)
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| dbo:icd10
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| dbo:medicalCause
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| dbo:medicalDiagnosis
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| dbo:omim
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| dbo:symptom
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| dbo:thumbnail
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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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- Mutations in PHKA1, PHKA2, PHKB, or PHKG2 genes (en)
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| dbp:diagnosis
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| dbp:genereviewsname
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- Phosphorylase Kinase Deficiency (en)
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| dbp:genereviewsnbk
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| dbp:icd
| |
| dbp:name
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- Glycogen storage disease IX (en)
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| dbp:omim
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| dbp:symptoms
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| dbp:treatment
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- Physical therapy, follow metabolic nutritionist (en)
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| dbp:wikiPageUsesTemplate
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| dbp:wordnet_type
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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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- Glycogen storage disease type IX (en)
- Glykogenose Typ IX (de)
- Болезнь Хага (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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- Glycogen storage disease IX (en)
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| is dbo:wikiPageWikiLink
of | |
| is foaf:primaryTopic
of | |
