Parkinson's disease 23

Summary
Synonym
  • autosomal recessive early-onset Parkinson disease 23
  • autosomal recessive early-onset Parkinson's disease 23
Definition
An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.
Super Class
autosomal recessive disease early-onset Parkinson's disease
External Links
Disease Ontology
DOID:0060896
Mondo Disease Ontology
OMIM
Related Genes
Displaying entries 131 - 140 of 164 in total
Gene ID Gene Symbol Description Source
11343 MGLL monoglyceride lipase
22876 INPP5F inositol polyphosphate-5-phosphatase F
22933 SIRT2 sirtuin 2
23098 SARM1 sterile alpha and TIR motif containing 1
23205 ACSBG1 acyl-CoA synthetase bubblegum family member 1
23583 SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
26232 FBXO2 F-box protein 2
27036 SIGLEC7 sialic acid binding Ig like lectin 7
27087 B3GAT1 beta-1,3-glucuronyltransferase 1
27306 HPGDS hematopoietic prostaglandin D synthase
The Human Phenotype Ontology
Displaying entries 11 - 20 of 31 in total
HPO ID HPO Term
HP:0001257 Spasticity
HP:0001332 Dystonia
HP:0001337 Tremor
HP:0001347 Hyperreflexia
HP:0002014 Diarrhea
HP:0002018 Nausea
HP:0002019 Constipation
HP:0002063 Rigidity
HP:0002067 Bradykinesia
HP:0002141 Gait imbalance
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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