About: urea cycle disorder

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	amino acid metabolic disorder
label	urea cycle disorder
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:9267
database_cross_reference	GARD:7837 ICD10CM:E72.2 ICD9CM:270.6 MESH:D056806 NCI:C84785 SNOMEDCT_US_2021_09_01:36444000 UMLS_CUI:C0154246
has_exact_synonym	disorder of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia (en) disorder of urea cycle metabolism (en) urea cycle defect (en)
has_obo_namespace	disease_ontology
in_subset	NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	An amino acid metabolic disorder that involves a deficiency of one of the enzymes in the urea cycle which is responsible for removing ammonia from the blood stream.
is subClassOf of	ornithine carbamoyltransferase deficiency hyperargininemia carbamoyl phosphate synthetase I deficiency disease N-acetylglutamate synthase deficiency citrullinemia
is someValuesFrom of	nodeID://b50956442
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50956429

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