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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Human disease

AttributesValues
rdf:type
owl:sameAs
description
  • Krankheit (de)
  • Human disease (en)
  • maladie (fr)
  • malattia (it)
  • մարդու հիվանդություն (hy)
  • хвороба людини (uk)
  • مرض يصيب الإنسان (ar)
exact match
exact match
Mondo ID
Disease Ontology ID
Mondo ID
Disease Ontology ID
Mondo ID
  • MONDO_0012277
Disease Ontology ID
  • DOID:0080095
rdfs:label
  • myofibrillar myopathy 4 (en)
  • myopathie distale tardive type Markesbery-Griggs (fr)
skos:prefLabel
  • myofibrillar myopathy 4 (en)
  • myopathie distale tardive type Markesbery-Griggs (fr)
name
  • myofibrillar myopathy 4 (en)
  • myopathie distale tardive type Markesbery-Griggs (fr)
instance of
instance of
subclass of
subclass of
UniProt disease ID
Orphanet ID
genetic association
ICD-10-CM
GARD rare disease ID
OMIM ID
UniProt disease ID
  • DI-02467
Orphanet ID
  • 98912
genetic association
ICD-10-CM
  • G71.8
GARD rare disease ID
  • 1886
OMIM ID
  • 609452
skos:altLabel
  • MFM4 (en)
  • ZASP (fr)
  • Late-onset distal myopathy, Markesbery-Griggs type (en)
  • MYOPATHY, MYOFIBRILLAR, 4 (en)
  • MYOPATHY, MYOFIBRILLAR, 4; MFM4 (en)
  • Myopathy, Myofibrillar, type 4 (en)
  • ZASP-related myofibrillar myopathy (en)
  • myofibrillar myopathy type 4 (en)
  • myopathie myofibrillaire type 4 (fr)
  • zaspopathie (fr)
  • zaspopathy (en)
UMLS CUI
MeSH descriptor ID
on focus list of Wikimedia project
Microsoft Academic ID
MeSH descriptor ID
Microsoft Academic ID
UMLS CUI
  • C1836155
MeSH descriptor ID
  • C563718
on focus list of Wikimedia project
Microsoft Academic ID
  • 2778717455
is about of
is genetic association of
is genetic association of
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