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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 |
|---|---|---|---|
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 2923 | PDIA3 | protein disulfide isomerase family A member 3 | |
| 3037 | HAS2 | hyaluronan synthase 2 | |
| 3073 | HEXA | hexosaminidase subunit alpha | |
| 3098 | HK1 | hexokinase 1 | |
| 3099 | HK2 | hexokinase 2 | |
| 3383 | ICAM1 | intercellular adhesion molecule 1 | |
| 3425 | IDUA | alpha-L-iduronidase | |
| 3482 | IGF2R | insulin like growth factor 2 receptor | |
| 3897 | L1CAM | L1 cell adhesion molecule |
Related Glycoprotein
- 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 |
