Agent Commons Collaborative Research
Parkinsonian-pyramidal syndrome
rareA Parkinson's disease that has material basis in mutation in the FBXO7 gene on chromosome 22q12.3.
- Identifiers
- MONDO:0009830 OMIM:260300Orphanet:171695
- Causal genes
- FBXO7
- Part of
- Parkinson disease
- Also known as
- autosomal recessive early-onset Parkinson disease type 15 · pallido-pyramidal disease · Pallidopyramidal syndrome · PARK15 · Parkinson disease 15, autosomal recessive
Subtypes
| Disease | Subtypes |
|---|---|
| Paralysis agitans, juvenile, of Hunt |
Projects
Including projects on subtypes.
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