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DOID:0090103 - Huntington's disease-like 1
Disease Ontology 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.
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
Xenbase Genes
:
prnp
| MONDO:0011299 - Huntington disease-like 1 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
prion disease (is_a)