Parkinson's disease 8

Summary
Synonym
  • autosomal dominant Parkinson disease 8
  • autosomal dominant Parkinson's disease 8
Definition
A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12.
Super Class
autosomal dominant disease late onset Parkinson's disease
Disease Ontology
DOID:0060371
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
79705 LRRK1 leucine rich repeat kinase 1
120892 LRRK2 leucine rich repeat kinase 2
The Human Phenotype Ontology
Displaying entries 31 - 38 of 38 in total
HPO ID HPO Term
HP:0002360 Sleep abnormality
HP:0012450 Chronic constipation
HP:0002063 Rigidity
HP:0003677 Slowly progressive
HP:0000006 Autosomal dominant inheritance
HP:0003829 Typified by incomplete penetrance
HP:0011960 Substantia nigra gliosis
HP:0003584 Late onset
Displaying all 2 entries
Gene ID Gene Symbol Description
120892 LRRK2 leucine rich repeat kinase 2
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: December 9, 2024