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About:
peroxisomal acyl-CoA oxidase deficiency
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An Entity of Type :
owl:Class
, within Data Space :
demo.openlinksw.com
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Class
subClassOf
peroxisomal disease
label
peroxisomal acyl-CoA oxidase deficiency
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0050797
created_by
lschriml
creation_date
2013-11-21T10:47:41Z
database_cross_reference
MESH:C536662
NCI:C170437
OMIM:264470
SNOMEDCT_US_2021_09_01:238069004
UMLS_CUI:C1849678
has_exact_synonym
Peroxisomal acyl-coenzyme A oxidase
(en)
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
A peroxisomal disease that is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50937618
Faceted Search & Find service v1.17_git151 as of Feb 20 2025
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