OBO ID: DOID:0090103 |
Term Name: | Huntington's disease-like 1 | Search Ontology: | |
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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) | ||
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Ontology: | Human Disease ( DOID:0090103 ) |
OTHER Huntington's disease-like 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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