Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / OrganismsTools
SugarDrawer
GlycanBuilder
Glycan Converters
GlycoMaple
GlycomeAtlas
LM-GlycomeAtlas
GALAXY
MCAW
GlycoSim
GRable
Guidelines
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:0001260 | Dysarthria |
| HP:0012675 | Iron accumulation in brain |
| HP:0001337 | Tremor |
| HP:0000746 | Delusion |
| HP:0002312 | Clumsiness |
| HP:0000338 | Hypomimic face |
| HP:0001347 | Hyperreflexia |
| HP:0002548 | Parkinsonism with favorable response to dopaminergic medication |
| HP:0000751 | Personality changes |
| HP:0007153 | Progressive extrapyramidal movement disorder |
