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About:
hyperekplexia
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Class
subClassOf
nervous system disease
label
hyperekplexia
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0060695
database_cross_reference
ICD10CM:G25.8
OMIM:PS149400
ORDO:3197
has_exact_synonym
Kok disease
(en)
congenital stiff man syndrome
(en)
familial startle disease
(en)
hereditary hyperekplexia
(en)
startle disease
(en)
has_obo_namespace
disease_ontology
in_subset
DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115
A nervous system disease characterized by an exaggerated startle response to sudden, unexpected auditory or tactile stimuli and hypertonia.
is
subClassOf
of
hyperekplexia 1
hyperekplexia 2
hyperekplexia 3
hyperekplexia 4
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50939219
Faceted Search & Find service v1.17_git144 as of Jul 26 2024
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