Phenotypes for disease #03122 (SPG35 (paraplegia, spastic, autosomal recessive, type 35 (SPG-35)), OMIM:612319)

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Individual ID     
0000296642 52-y man with progressive spasticity and weakness of both lower limbs, cognitive impairment (mild/moderate) and slurred speech. HSP SPG35 Familial, autosomal recessive 52y - 35y - - Sherifa Ahmed Hamed 00404049
0000325651 Strabismus, Ataxia, Gait disturbance, Muscle weakness, Myoclonus, Brisk reflexes, Gait imbalance, Skeletal muscle atrophy, Myalgia, Babinski sign, Myoclonic spasms, Pontocerebellar atrophy, Hypoplasia of the pons, Low levels of vitamin D - - Familial, autosomal recessive 16y - - - - Andreas Laner 00435460
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