Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024

Preferred Name	Rare genetic cause of hypertension
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_156629
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=156629
hasDbXref	UMLS:C5680639
label	Rare genetic cause of hypertension
notation	ORPHA:156629 Category
prefixIRI	ORDO:Orphanet_156629
prefLabel	Rare genetic cause of hypertension
subClassOf	http://www.orpha.net/ORDO/Orphanet_98056 http://www.orpha.net/ORDO/Orphanet_93618 http://www.orpha.net/ORDO/Orphanet_557492

Delete	Subject	Author	Type	Created
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Delete	Mapping To	Ontology	Source
	http://www.orpha.net/ORDO/Orphanet_156629	EFO	SAME_URI