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Parkinson's disease 1
Summary
- Synonym
-
- autosomal dominant Parkinson disease 1
- autosomal dominant Parkinson's disease 1
- Definition
- A late onset Parkinson's disease that has_material_basis_in mutation in the alpha-synuclein gene on chromosome 4q22.1.
- Super Class
- autosomal dominant disease late onset Parkinson's disease
External Links
- Disease Ontology
- DOID:0060367
- Mondo Disease Ontology
- OMIM
- MGI genotype (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002171 | Gliosis |
| HP:0100710 | Impulsivity |
| HP:0001268 | Mental deterioration |
| HP:0002548 | Parkinsonism with favorable response to dopaminergic medication |
| HP:0000716 | Depression |
| HP:0002359 | Frequent falls |
| HP:0005340 | Spastic/hyperactive bladder |
| HP:0002015 | Dysphagia |
| HP:0000651 | Diplopia |
| HP:0002304 | Akinesia |
