About: myoclonic dystonia 15     Goto   Sponge   NotDistinct   Permalink

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myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11

AttributesValues
rdf:type
description
  • myoclonic dystonia characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 18p11 (en)
exact match
exact match
Mondo ID
Disease Ontology ID
Mondo ID
Disease Ontology ID
Mondo ID
  • MONDO_0011844
Disease Ontology ID
  • DOID:0090035
rdfs:label
  • myoclonic dystonia 15 (en)
skos:prefLabel
  • myoclonic dystonia 15 (en)
name
  • myoclonic dystonia 15 (en)
instance of
instance of
subclass of
subclass of
Orphanet ID
OMIM ID
Orphanet ID
  • 210566
OMIM ID
  • 607488
skos:altLabel
  • DYSTONIA 15, MYOCLONIC (en)
  • DYSTONIA 15, MYOCLONIC; DYT15 (en)
  • DYT15 (en)
  • myoclonic dystonia type 15 (en)
UMLS CUI
MeSH descriptor ID
on focus list of Wikimedia project
MeSH descriptor ID
UMLS CUI
  • C1843786
MeSH descriptor ID
  • C538002
on focus list of Wikimedia project
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