Parkinson's disease 4

Summary
Synonym
  • autosomal dominant Lewy body Parkinson disease 4
  • autosomal dominant Parkinson disease 4
  • autosomal dominant Parkinson's disease 4
Definition
A late onset Parkinson disease that has_material_basis_in heterozygous triplication of the alpha-synuclein gene on chromosome 4q22.
Super Class
autosomal dominant disease late onset Parkinson's disease
External Links
Disease Ontology
DOID:0060895
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 71 - 80 of 164 in total
Gene ID Gene Symbol Description Source
3956 LGALS1 galectin 1
3958 LGALS3 galectin 3
3960 LGALS4 galectin 4
4051 CYP4F3 cytochrome P450 family 4 subfamily F member 3
4099 MAG myelin associated glycoprotein
4360 MRC1 mannose receptor C-type 1
4669 NAGLU N-acetyl-alpha-glucosaminidase
4680 CEACAM6 CEA cell adhesion molecule 6
4907 NT5E 5'-nucleotidase ecto
4968 OGG1 8-oxoguanine DNA glycosylase
The Human Phenotype Ontology
Displaying entries 31 - 33 of 33 in total
HPO ID HPO Term
HP:0100660 Dyskinesia
HP:0100710 Impulsivity
HP:0100753 Schizophrenia
Displaying 1 entry
Gene ID Gene Symbol Description
2629 GBA1 glucosylceramidase beta 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024