http://schema.org/description
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syndrome that is characterized by progressive proximal muscle weakness, steolytic bone lesions consistent with Paget disease, and frontotemporal dementia and has physical basis in mutation in the valosin containing protein (VCP)
, malattia
, Krankheit
, хвороба
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http://schema.org/name
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syndrome myopathie à inclusions - maladie de Paget - démence fronto-temporale
, inclusion body myopathy with Paget disease of bone and frontotemporal dementia
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http://www.w3.org/2004/02/skos/core#altLabel
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Syndrome myopathie à inclusions - maladie de paget - démence fronto-temporale
, Syndrome myopathie a inclusions - maladie de Paget - demence fronto-temporale
, IBMPFD
, inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
, Limb-girdle muscular dystrophy with Paget disease of bone
, Pagetoid neuroskeletal syndrome
, inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia
, Pagetoid amyotrophic lateral sclerosis
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http://www.w3.org/2004/02/skos/core#prefLabel
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syndrome myopathie à inclusions - maladie de Paget - démence fronto-temporale
, inclusion body myopathy with Paget disease of bone and frontotemporal dementia
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G71.8
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10899
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615424
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H02031
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1947548457
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rdf:type |
http://wikiba.se/ontology#Item +
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rdfs:label |
syndrome myopathie à inclusions - maladie de Paget - démence fronto-temporale
, inclusion body myopathy with Paget disease of bone and frontotemporal dementia
|