Orphanet Rare Disease Ontology

Last uploaded: December 4, 2024

Preferred Name	Peroxisomal disease
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_68373
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=68373
hasDbXref	UMLS:C5681330 ICD-11:5C57 MeSH:D018901
label	Peroxisomal disease
notation	ORPHA:68373 Category
prefixIRI	ORDO:Orphanet_68373
prefLabel	Peroxisomal disease
subClassOf	http://www.orpha.net/ORDO/Orphanet_557492 http://www.orpha.net/ORDO/Orphanet_68367

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_68373	CCONT	SAME_URI
http://www.orpha.net/ORDO/Orphanet_68373	EFO	SAME_URI
http://purl.obolibrary.org/obo/DOID_906	DOID	LOOM
http://purl.obolibrary.org/obo/MONDO_0019053	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0019053	MONDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0019053	DOVES	LOOM
http://purl.obolibrary.org/obo/MONDO_0019053	KTAO	LOOM
http://purl.obolibrary.org/obo/MONDO_0019053	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0019053	OBA	LOOM
http://www.limics.org/hrdo/rdfns#pat_id_10513	HRDO	LOOM
http://purl.obolibrary.org/obo/DOID_906	DTO	LOOM
http://purl.obolibrary.org/obo/DOID_906	BAO	LOOM
http://purl.obolibrary.org/obo/DOID_906	EPIO	LOOM
http://purl.obolibrary.org/obo/DOID_906	HHEAR	LOOM
http://purl.obolibrary.org/obo/DOID_906	NIFSTD	LOOM
http://purl.obolibrary.org/obo/DOID_906	FNS-H	LOOM