[On the subject of a familial disease characterized by a predominantly distal amyotrophia, spasmodic paraparesis and, in certain members, mental changes and coordination disorders].
D001259:Ataxia; D006801:Humans; D001523:Mental Disorders / Q000235:genetics*; D009069:Movement Disorders / Q000235:genetics*; D009133:Muscular Atrophy / Q000235:genetics*; D010243:Paralysis / Q000235:genetics*; D020335:Paraparesis
MENTAL DISORDERS/genetics; MOVEMENT DISORDERS/genetics; MUSCULAR ATROPHY/genetics; PARALYSIS/genetics