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Parkinson's disease 19A
Summary
- Synonym
-
- juvenile onset Parkinson disease 19A
- juvenile onset Parkinson's disease 19A
- Definition
- An early-onset Parkinson's diseas that has_material_basis_in homozygous mutation in the DNAJC6 gene on chromosome 1p31.
- Super Class
- autosomal recessive disease early-onset Parkinson's disease
External Links
- Disease Ontology
- DOID:0060891
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 308 | ANXA5 | annexin A5 | |
| 353 | APRT | adenine phosphoribosyltransferase | |
| 410 | ARSA | arylsulfatase A | |
| 427 | ASAH1 | N-acylsphingosine amidohydrolase 1 | |
| 683 | BST1 | bone marrow stromal cell antigen 1 | |
| 811 | CALR | calreticulin | |
| 847 | CAT | catalase | |
| 929 | CD14 | CD14 molecule | |
| 952 | CD38 | CD38 molecule | |
| 960 | CD44 | CD44 molecule (IN blood group) |
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:0002322 | Resting tremor |
| HP:0002362 | Shuffling gait |
| HP:0002425 | Anarthria |
| HP:0002540 | Inability to walk |
| HP:0002578 | Gastroparesis |
| HP:0002650 | Scoliosis |
| HP:0003394 | Muscle spasm |
| HP:0004305 | Involuntary movements |
| HP:0004409 | Hyposmia |
| HP:0007164 | Slowed slurred speech |
