PhenomeGene — Human Disease Gene Website SeriesUFSP2

Clinical Characteristics

Neurologic disorder (p.V115E variant related)- associated with seizures, delayed motor and cognitive development.

Skeletal disorder (p.D426A, p.H428R, p.C302S variants)- short stature, bowing legs, asymmetric growth, spine deformity. Hip developmental disorder with the p.Y290H variant.