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Huntington's disease-like 1
Summary
- Synonym
-
- HDL1
- HLN1
- Huntington disease-like 1
- Huntington-like neurodegenerative disorder 1
- autosomal dominant Huntington-like neurodegenerative disorder
- early-onset prion disease with prominent psychiatric features
- Definition
- A prion disease that is characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has_material_basis_in autosomal dominant inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13.
- Super Class
- prion disease
External Links
- Disease Ontology
- DOID:0090103
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1718 | DHCR24 | 24-dehydrocholesterol reductase | |
| 2215 | FCGR3B | Fc gamma receptor IIIb | |
| 2572 | GAD2 | glutamate decarboxylase 2 | |
| 2597 | GAPDH | glyceraldehyde-3-phosphate dehydrogenase | |
| 2739 | GLO1 | glyoxalase I | |
| 2882 | GPX7 | glutathione peroxidase 7 | |
| 2997 | GYS1 | glycogen synthase 1 | |
| 3417 | IDH1 | isocitrate dehydrogenase (NADP(+)) 1 | |
| 3425 | IDUA | alpha-L-iduronidase | |
| 3958 | LGALS3 | galectin 3 |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002066 | Gait ataxia |
| HP:0002067 | Bradykinesia |
| HP:0002072 | Chorea |
| HP:0002119 | Ventriculomegaly |
| HP:0002120 | Cerebral cortical atrophy |
| HP:0002134 | Abnormal basal ganglia morphology |
| HP:0002171 | Gliosis |
| HP:0002311 | Incoordination |
| HP:0002312 | Clumsiness |
| HP:0002353 | EEG abnormality |
