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About:
immunodeficiency 39
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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
primary immunodeficiency disease
nodeID://b50945832
label
immunodeficiency 39
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0111969
database_cross_reference
OMIM:616345
has_exact_synonym
IMD39
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
A primary immunodeficiency disease characterized by impaired interferon I and III production in response to influenza virus infection that has_material_basis_in homozygous or compond heterozygous mutation in IRF7 on chromosome 11p15.5.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50945833
Faceted Search & Find service v1.17_git144 as of Jul 26 2024
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