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About:
peroxisomal disease
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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
inherited metabolic disorder
label
peroxisomal disease
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:906
database_cross_reference
ICD10CM:E71.5
ICD9CM:277.86
MESH:D018901
NCI:C85005
SNOMEDCT_US_2021_09_01:238059005
UMLS_CUI:C0282528
has_exact_synonym
peroxisomal disorder
(en)
has_obo_namespace
disease_ontology
in_subset
DO_FlyBase_slim
NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115
An inherited metabolic disorder that involves peroxisome malfunction.
is
subClassOf
of
acatalasia
infantile Refsum disease
mevalonic aciduria
peroxisomal acyl-CoA oxidase deficiency
alpha-methylacyl-CoA racemase deficiency
peroxisomal biogenesis disorder
retinal dystrophy with leukodystrophy
D-bifunctional protein deficiency
glutaric acidemia type 3
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50956256
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