Huntington disease
- Subj. Area:
-
V
Medicine and Care
IX Genetics, Human Reproduction and Sexuality - Ger:
- Chorea Huntington
- Fr:
- maladie de Huntington
- SN:
- A familial disorder inherited as an autosomal dominant trait and characterised by the onset of progressive chorea (involuntary and irregular movement) and dementia in the fourth or fifth decade of life (based on MeSH-2007)
- UF:
-
Huntington chorea
Huntington's disease
- RT:
-
brain diseases
- Conc:
-
B: Huntington disease
E: Huntington's disease
I: maladie de Huntington
M: Huntington Disease (D006816)
