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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 |
|---|---|---|---|
| 64116 | SLC39A8 | solute carrier family 39 member 8 | |
| 64132 | XYLT2 | xylosyltransferase 2 | |
| 65078 | RTN4R | reticulon 4 receptor | |
| 79154 | DHRS11 | dehydrogenase/reductase 11 | |
| 79661 | NEIL1 | nei like DNA glycosylase 1 | |
| 79993 | ELOVL7 | ELOVL fatty acid elongase 7 | |
| 80270 | HSD3B7 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | |
| 80351 | TNKS2 | tankyrase 2 | |
| 132789 | GNPDA2 | glucosamine-6-phosphate deaminase 2 | |
| 151056 | PLB1 | phospholipase B1 |
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 |
