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