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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
  • Huntington's disease-like 1
described by
id
  • DOID:0090103
database_cross_reference
  • ICD10CM:G10
  • OMIM:603218
  • ORDO:157941
has_exact_synonym
  • HDL1 (en)
  • HLN1 (en)
  • Huntington disease-like 1 (en)
  • Huntington-like neurodegenerative disorder 1 (en)
  • autosomal dominant Huntington-like neurodegenerative disorder (en)
  • early-onset prion disease with prominent psychiatric features (en)
has_obo_namespace
  • disease_ontology
http://purl.obolib...g/obo/IAO_0000115
  • A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13.
is topic of
is annotatedSource of
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