Kufor-Rakeb syndrome

Summary
Synonym
  • autosomal recessive Parkinson disease 9
  • autosomal recessive juvenile onset Parkinson disease 9
Definition
An early-onset Parkinson's disease that is characterized by supranuclear gaze palsy, spasticity, and dementia and has_material_basis_in homozygous or compound heterozygous mutation in a lysosomal type 5 ATPase encoding gene on chromosome 1p36.
Super Class
autosomal recessive disease early-onset Parkinson's disease
Disease Ontology
DOID:0060556
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
23400 ATP13A2 ATPase cation transporting 13A2
79572 ATP13A3 ATPase 13A3
344905 ATP13A5 ATPase 13A5
Displaying all 3 entries
Gene ID Gene Symbol Description Source
74772 Atp13a2 ATPase type 13A2
224088 Atp13a3 ATPase type 13A3
268878 Atp13a5 ATPase type 13A5

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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