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Huntington disease

^ http://www.orpha.net/ORDO/Orphanet_399


Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia.

Synonyms: Huntington chorea

Term info

database cross reference
  • MedDRA:10070668 (E (exact mapping (the terms and the concepts are equivalent)))
  • MeSH:D006816 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:143100 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:G10 (Specific code (The term has its own code in the ICD10))
  • UMLS:C0020179 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:G10 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

MedDRA:10070668, ICD-10:G10, UMLS:C0020179, MeSH:D006816, OMIM:143100

notation

ORPHA:399

Term relations

Subclass of: