Parkinson's disease 19A

Summary
Synonym
  • juvenile onset Parkinson disease 19A
  • juvenile onset Parkinson's disease 19A
Definition
An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.
Super Class
autosomal recessive disease early-onset Parkinson's disease
External Links
Disease Ontology
DOID:0060891
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying entries 41 - 50 of 164 in total
Gene ID Gene Symbol Description Source
1738 DLD dihydrolipoamide dehydrogenase
1800 DPEP1 dipeptidase 1
2026 ENO2 enolase 2
2053 EPHX2 epoxide hydrolase 2
2194 FASN fatty acid synthase
2203 FBP1 fructose-bisphosphatase 1
2208 FCER2 Fc epsilon receptor II
2215 FCGR3B Fc gamma receptor IIIb
2539 G6PD glucose-6-phosphate dehydrogenase
2571 GAD1 glutamate decarboxylase 1
The Human Phenotype Ontology
Displaying entries 31 - 40 of 54 in total
HPO ID HPO Term
HP:0002322 Resting tremor
HP:0002362 Shuffling gait
HP:0002425 Anarthria
HP:0002540 Inability to walk
HP:0002578 Gastroparesis
HP:0002650 Scoliosis
HP:0003394 Muscle spasm
HP:0004305 Involuntary movements
HP:0004409 Hyposmia
HP:0007164 Slowed slurred speech
Displaying 1 entry
Gene ID Gene Symbol Description
8867 SYNJ1 synaptojanin 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