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Parkinsonian-pyramidal syndrome
MONDO:0009830A Parkinson's disease that has material basis in mutation in the FBXO7 gene on chromosome 22q12.3.
Also known as: Pallidopyramidal syndrome, Parkinson disease 15, autosomal recessive, autosomal recessive early-onset Parkinson disease type 15, pallidopyramidal syndrome, parkinsonian-pyramidal syndrome, PARK15, Parkinson disease 15, autosomal recessive early-onset, autosomal recessive early-onset Parkinson's disease 15
12 clinical trials for this condition and its sub-types, 0 tagged with Parkinsonian-pyramidal syndrome itself.
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Sub-types of Parkinsonian-pyramidal syndrome
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Paralysis agitans, juvenile, of Hunt 0 trials
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