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Parkinson's disease 7
Summary
- Synonym
-
- autosomal recessive early-onset Parkinson disease 7
- autosomal recessive early-onset Parkinson's disease 7
- Definition
- An early-onset Parkinson's disease that has_material_basis_in homozygous or compound heterozygous mutation in the DJ1 gene on chromosome 1p36.
- Super Class
- autosomal recessive disease early-onset Parkinson's disease
External Links
- Disease Ontology
- DOID:0060370
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q99497 | Parkinson disease protein 7 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q99LX0 | Parkinson disease protein 7 homolog |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002018 | Nausea |
| HP:0000738 | Hallucinations |
| HP:0004409 | Hyposmia |
| HP:0000716 | Depression |
| HP:0002141 | Gait imbalance |
| HP:0100543 | Cognitive impairment |
| HP:0001332 | Dystonia |
| HP:0000651 | Diplopia |
| HP:0002063 | Rigidity |
| HP:0012452 | Restless legs |
