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DO Term : Huntington's disease-like 1 [DOID:0090103] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • ICD10CM:G10,
  • HDL1,
  • ORDO:157941,
  • OMIM:603218,
  • autosomal dominant Huntington-like neurodegenerative disorder,
  • HLN1,
  • Huntington disease-like 1,
  • early-onset prion disease with prominent psychiatric features,
  • Huntington-like neurodegenerative disorder 1,
  • 603218
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents