Orphanet Rare Disease Ontology

Last uploaded: December 4, 2024

Preferred Name	Familial restrictive cardiomyopathy
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_217635
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=217635
hasDbXref	UMLS:C0340429
label	Familial restrictive cardiomyopathy
notation	ORPHA:217635 Category
prefixIRI	ORDO:Orphanet_217635
prefLabel	Familial restrictive cardiomyopathy
subClassOf	http://www.orpha.net/ORDO/Orphanet_557492 http://www.orpha.net/ORDO/Orphanet_217632 http://www.orpha.net/ORDO/Orphanet_98054

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_217635	CCONT	SAME_URI
http://www.orpha.net/ORDO/Orphanet_217635	EFO	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0016340	MONDO	LOOM
http://purl.bioontology.org/ontology/RCD/X201e	RCD	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/233878008	SNOMEDCT	LOOM
http://purl.obolibrary.org/obo/MONDO_0016340	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0016340	DOVES	LOOM
http://purl.obolibrary.org/obo/MONDO_0016340	KTAO	LOOM
http://purl.obolibrary.org/obo/MONDO_0016340	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0016340	OBA	LOOM
http://www.limics.org/hrdo/rdfns#pat_id_18882	HRDO	LOOM