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inflammatory muscle disease in older adults

AttributesValues
rdf:type
description
  • sjukdom (sv)
  • systémové zánětlivé onemocnění pojivové tkáně (cs)
  • Muskelkrankheit (de)
  • Spierziekte (nl)
  • doença inflamatória (pt)
  • forma di miosite di tipo infiammatorio (it)
  • inflammatory muscle disease in older adults (en)
exact match
exact match
health specialty
DiseasesDB
Disease Ontology ID
symptoms and signs
Disease Ontology ID
health specialty
DiseasesDB
  • 30691
Disease Ontology ID
  • DOID:3429
symptoms and signs
rdfs:label
  • Inklusjonslegememyositt (nb)
  • Miositis por cuerpos de inclusión (es)
  • Sporadische Einschlusskörpermyositis (de)
  • Wtrętowe zapalenie mięśni (pl)
  • inclusion body myositis (en)
  • inclusion body myositis (nl)
  • inklusionskroppsmyosit (sv)
  • miosite da corpi inclusi (it)
  • miosite por corpúsculos de inclusão (pt)
  • myosite à inclusions (fr)
  • myositida s inkluzními tělísky (cs)
  • التهاب العضلات المشتمل (ar)
  • 包涵體肌炎 (zh)
  • 封入体筋炎 (ja)
  • 포함체 근육염 (ko)
skos:prefLabel
  • Inklusjonslegememyositt (nb)
  • Miositis por cuerpos de inclusión (es)
  • Sporadische Einschlusskörpermyositis (de)
  • Wtrętowe zapalenie mięśni (pl)
  • inclusion body myositis (en)
  • inclusion body myositis (nl)
  • inklusionskroppsmyosit (sv)
  • miosite da corpi inclusi (it)
  • miosite por corpúsculos de inclusão (pt)
  • myosite à inclusions (fr)
  • myositida s inkluzními tělísky (cs)
  • التهاب العضلات المشتمل (ar)
  • 包涵體肌炎 (zh)
  • 封入体筋炎 (ja)
  • 포함체 근육염 (ko)
name
  • Inklusjonslegememyositt (nb)
  • Miositis por cuerpos de inclusión (es)
  • Sporadische Einschlusskörpermyositis (de)
  • Wtrętowe zapalenie mięśni (pl)
  • inclusion body myositis (en)
  • inclusion body myositis (nl)
  • inklusionskroppsmyosit (sv)
  • miosite da corpi inclusi (it)
  • miosite por corpúsculos de inclusão (pt)
  • myosite à inclusions (fr)
  • myositida s inkluzními tělísky (cs)
  • التهاب العضلات المشتمل (ar)
  • 包涵體肌炎 (zh)
  • 封入体筋炎 (ja)
  • 포함체 근육염 (ko)
Freebase ID
Freebase ID
  • /m/03_1n
instance of
instance of
subclass of
subclass of
eMedicine ID
eMedicine ID
  • 1172746
KEGG ID
has cause
KEGG ID
KEGG ID
  • H01505
has cause
prevalence
Orphanet ID
ICD-9-CM
genetic association
ICD-10-CM
PatientsLikeMe condition ID
GARD rare disease ID
OMIM ID
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