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Disease Ontology Browser
Huntington's disease-like 1 (DOID:0090103)
Alliance: disease page
Synonyms: 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
Alt IDs: OMIM:603218, ICD10CM:G10, ORDO:157941
Definition: A prion disease characterized by a phenocopy of Huntington disease (unwanted choreatic movements, behavioral and psychiatric disturbances and dementia) that has material_basis_in the presence of 8 extra octapeptide repeats in the PRNP gene on chromosome 20p13.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/12/2019
MGI 6.13
The Jackson Laboratory