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About:
Usher syndrome type 2
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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
Usher syndrome
label
Usher syndrome type 2
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0110827
database_cross_reference
MESH:D052245
NCI:C126328
ORDO:231178
SNOMEDCT_US_2020_03_01:232058008
has_exact_synonym
USH2
(en)
has_obo_namespace
disease_ontology
in_subset
NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115
An Usher syndrome characterized by mild to severe congenital hearing impairment, normal vestibular function and later development of retinitis pigmentosa.
is
subClassOf
of
Usher syndrome type 2A
Usher syndrome type 2C
Usher syndrome type 2D
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50943738
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