A neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.

Synonyms: Huntington's chorea Huntington disease HD

This is just here as a test because I lose it

Term information

database cross reference
  • NCI:C82342
  • GARD:6677
  • UMLS_CUI:C0020179
  • SNOMEDCT_US_2020_03_01:155006000
  • KEGG:05016
  • OMIM:143100
  • ICD10CM:G10
  • ICD9CM:333.4
  • MESH:D006816
  • SNOMEDCT_US_2020_09_01:155006000
Subsets

DO_FlyBase_slim, NCIthesaurus

database cross reference

NCI:C82342

ICD10CM:G10

SNOMEDCT_US_2020_09_01:155006000

GARD:6677

SNOMEDCT_US_2020_03_01:155006000

ICD9CM:333.4

KEGG:05016

MESH:D006816

OMIM:143100

UMLS_CUI:C0020179

has obo namespace

disease_ontology

id

DOID:12858

imported from

http://purl.obolibrary.org/obo/doid.owl

Term relations