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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
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 6470 | SHMT1 | serine hydroxymethyltransferase 1 | |
| 6472 | SHMT2 | serine hydroxymethyltransferase 2 | |
| 6476 | SI | sucrase-isomaltase | |
| 6517 | SLC2A4 | solute carrier family 2 member 4 | |
| 6609 | SMPD1 | sphingomyelin phosphodiesterase 1 | |
| 6610 | SMPD2 | sphingomyelin phosphodiesterase 2 | |
| 6646 | SOAT1 | sterol O-acyltransferase 1 | |
| 6888 | TALDO1 | transaldolase 1 | |
| 6900 | CNTN2 | contactin 2 | |
| 7086 | TKT | transketolase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P20815 | Cytochrome P450 3A5 | |
| P20916 | Myelin-associated glycoprotein | |
| P21399 | Cytoplasmic aconitate hydratase | |
| P21589 | 5'-nucleotidase | |
| P21964 | Catechol O-methyltransferase | |
| P22303 | Acetylcholinesterase | |
| P22897 | Macrophage mannose receptor 1 | |
| P27797 | Calreticulin | |
| P28329 | Choline O-acetyltransferase | |
| P28907 | ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 |
- The Human Phenotype Ontology
| 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 |
