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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

AttributesValues
type
subClassOf
label
  • dystonia 12
described by
id
  • DOID:0090056
database_cross_reference
  • ICD10CM:G24.1
  • OMIM:128235
  • ORDO:71517
has_obo_namespace
  • disease_ontology
http://purl.obolib...g/obo/IAO_0000115
  • A dystonia that is characterized by asymmetric dystonia and parkinsonism with abrupt onset in young adulthood that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the gene encoding the alpha-3 subunit of the N,K-ATPase (ATP1A3) on chromosome 19q13.
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