- Huntington's disease-like 1 [DOID:0090103]
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.
- chronic fatigue syndrome [DOID:8544]
A syndrome that involves prolonged and severe tiredness or weariness that is unrelated to exertion, is not relieved by rest and for a minimum of six months and is not directly caused by other conditions.
- myopathy [DOID:423]
A muscular disease in which the muscle fibers do not function resulting in muscular weakness.