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- B07343df03476fe36c4b2a3829e056a4e hasDbXref "MESH:D002527" @default.
- B07343df03476fe36c4b2a3829e056a4e type Axiom @default.
- B07343df03476fe36c4b2a3829e056a4e annotatedProperty IAO_0000115 @default.
- B07343df03476fe36c4b2a3829e056a4e annotatedSource MONDO_0008945 @default.
- B07343df03476fe36c4b2a3829e056a4e annotatedTarget "A condition marked by progressive cerebellar ataxia combined with myoclonus usually presenting in the third decade of life or later. Additional clinical features may include generalized and focal seizures, spasticity, and dyskinesias. Autosomal recessive and autosomal dominant patterns of inheritance have been reported. Pathologically, the dentate nucleus and brachium conjunctivum of the cerebellum are atrophic, with variable involvement of the spinal cord, cerebellar cortex, and basal ganglia. (From Joynt, Clinical Neurology, 1991, Ch37, pp60-1)" @default.