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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

Xenbase Genes : prnp

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011299 - Huntington disease-like 1

OMIM:
OMIM: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
Parent(s): prion disease (is_a)