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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 |
|---|---|---|
| Q9Y286 | Sialic acid-binding Ig-like lectin 7 | |
| Q9Y2H2 | Phosphatidylinositide phosphatase SAC2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0100785 | Insomnia |
