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MIRAGE
Parkinson's disease 14
Summary
- Synonym
-
- Dystonia-Parkinsonism Adult-Onset
- autosomal recessive Parkinson disease 14
- autosomal recessive Parkinson's disease 14
- Definition
- A late-onset Parkinson disease that has_material_basis_in homozygous mutation in the PLA2G6 gene on chromosome 22q13.
- Super Class
- autosomal recessive disease late onset Parkinson's disease
External Links
- Disease Ontology
- DOID:0060900
- Mondo Disease Ontology
- MeSH
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P97819 | 85/88 kDa calcium-independent phospholipase A2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002015 | Dysphagia |
| HP:0001250 | Seizure |
| HP:0004373 | Focal dystonia |
| HP:0000658 | Eyelid apraxia |
| HP:0002172 | Postural instability |
| HP:0010522 | Dyslexia |
| HP:0001332 | Dystonia |
| HP:0000571 | Hypometric saccades |
| HP:0002067 | Bradykinesia |
| HP:0007058 | Generalized cerebral atrophy/hypoplasia |
