Search Ontology:
Human Disease
Huntington's disease-like 1
- Term ID
- DOID:0090103
- Synonyms
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- autosomal dominant Huntington-like neurodegenerative disorder
- early-onset prion disease with prominent psychiatric features
- HDL1
- HLN1
- Huntington disease-like 1
- Huntington-like neurodegenerative disorder 1
- 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. (2)
- References
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- ICD10CM:G10
- MIM:603218
- ORDO:157941
- Ontology
- Human Disease ( DOID:0090103 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models