International Classification of Diseases, Version 10 - Clinical Modification - Hereditary xanthinuria - Classes

Last uploaded: January 16, 2025

Preferred Name	Hereditary xanthinuria
Synonyms
ID	http://purl.bioontology.org/ontology/ICD10CM/E79.82
cui	C5779508
notation	E79.82
Order number	04991
prefLabel	Hereditary xanthinuria
tui	T047
subClassOf	http://purl.bioontology.org/ontology/ICD10CM/E79.8

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/SNMI/D6-40500	SNMI	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/54627004	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/SCTSPA/54627004	SCTSPA	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/54627004	SNOMEDCT	LOOM
http://www.orpha.net/ORDO/Orphanet_3467	ORDO	LOOM
http://purl.jp/bio/4/id/200906060127388350	IOBC	LOOM
http://www.limics.org/hrdo/rdfns#pat_id_704	HRDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0018106	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0018106	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0018106	MONDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0018106	DOVES	LOOM
http://purl.obolibrary.org/obo/MONDO_0018106	KTAO	LOOM
http://purl.obolibrary.org/obo/MONDO_0018106	OBA	LOOM