Cell Culture Ontology

Last uploaded: July 23, 2014
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Id http://purl.obolibrary.org/obo/MONDO_0011299
http://purl.obolibrary.org/obo/MONDO_0011299
Preferred Name

Huntington disease-like 1
Definitions
Any neurodegenerative disease with chorea in which the cause of the disease is a mutation in the PRNP gene.
Synonyms
prion disease, early-onset, with prominent psychiatric features
Huntington's disease-like 1
Huntington-like neurodegenerative disorder, autosomal dominant
early-onset prion disease with prominent psychiatric features
Huntington-like neurodegenerative disorder 1
Huntington disease-like type 1
PRNP neurodegenerative disease with chorea
neurodegenerative disease with chorea caused by mutation in PRNP
autosomal dominant Huntington-like neurodegenerative disorder
Huntington disease-like 1
HDL1
HLN1
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Type http://www.w3.org/2002/07/owl#Class

All Properties

definition

Any neurodegenerative disease with chorea in which the cause of the disease is a mutation in the PRNP gene.
preferred label
Huntington disease-like 1
label
Huntington disease-like 1
prefLabel
Huntington disease-like 1
database_cross_reference
MESH:C566398
Orphanet:157941
MEDGEN:355137
DOID:0090103
OMIM:603218
UMLS:C1864112
GARD:16985
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IAO_0000233
notation
MONDO:0011299
in_subset
has_related_synonym
prion disease, early-onset, with prominent psychiatric features
Huntington's disease-like 1
Huntington-like neurodegenerative disorder, autosomal dominant
id
MONDO:0011299
skos_exactMatch
subClassOf
type
has_exact_synonym
early-onset prion disease with prominent psychiatric features
Huntington-like neurodegenerative disorder 1
Huntington disease-like type 1
PRNP neurodegenerative disease with chorea
neurodegenerative disease with chorea caused by mutation in PRNP
autosomal dominant Huntington-like neurodegenerative disorder
Huntington disease-like 1
HDL1
HLN1
See more
See less
excluded_subClassOf
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