Huntington'S Disease-Like 1
Disease ID: disease_node_15362
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:G10, MIM:603218, ORDO:157941 |
|---|---|
| Subclassof | DOID_649 |
| Data Source | DOID |
| Synonyms | 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 |
| Doid Label | Huntington's disease-like 1 |
| Doid Description | 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 domit inheritance of 8 extra octapeptide repeats in the prion protein (PRNP) gene on chromosome 20p13. |
| Disease Node Id | disease_node_15362 |
| Doid Id | DOID_0090103 |
| Label | Huntington'S Disease-Like 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Prion Diseases(ID:disease_node_9041) (Disease)