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About:
autosomal dominant nonsyndromic deafness 40
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
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Attributes
Values
type
Class
subClassOf
autosomal dominant nonsyndromic deafness
label
autosomal dominant nonsyndromic deafness 40
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0110566
database_cross_reference
ICD10CM:H90.3
OMIM:616357
has_exact_synonym
DFNA40
(en)
autosomal dominant deafness 40
(en)
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CRYM gene on chromosome 16p12.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50943249
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