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
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
8398 PLA2G6 phospholipase A2 group VI
The Human Phenotype Ontology
Displaying entries 21 - 30 of 52 in total
HPO ID HPO Term
HP:0001263 Global developmental delay
HP:0000605 Supranuclear gaze palsy
HP:0002145 Frontotemporal dementia
HP:0011999 Paranoia
HP:0002063 Rigidity
HP:0001257 Spasticity
HP:0006892 Frontotemporal cerebral atrophy
HP:0000716 Depression
HP:0002185 Neurofibrillary tangles
HP:0001336 Myoclonus
Displaying 1 entry
Gene ID Gene Symbol Description
8398 PLA2G6 phospholipase A2 group VI

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024