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About:
long QT syndrome 12
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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
autosomal dominant disease
long QT syndrome
nodeID://b50943373
label
long QT syndrome 12
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0110653
database_cross_reference
ICD10CM:I45.8
OMIM:612955
has_exact_synonym
LQT12
(en)
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50943374
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