Summary Literature (0)

DOID:0090103 - Huntington disease-like 1

Disease Ontology 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.

Synonyms: HDL1, HLN1, Huntington-like neurodegenerative disorder 1, autosomal dominant Huntington-like neurodegenerative disorder, early-onset prion disease with prominent psychiatric features,

Echinobase Genes :


OMIM:

MIM:603218 - huntington disease-like 1; hdl1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee