Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024

Preferred Name	OBSOLETE: Genodermatosis with ocular features
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_98696
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=98696
label	OBSOLETE: Genodermatosis with ocular features
notation	ORPHA:98696
prefixIRI	ORDO:Orphanet_98696
prefLabel	OBSOLETE: Genodermatosis with ocular features
reason_for_obsolescence	This entity has been obsoleted from the Orphanet nomenclature of rare diseases.This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.Instead, consider using Rare genetic skin disease
subClassOf	http://www.orpha.net/ORDO/Orphanet_C051

Delete	Subject	Author	Type	Created
No notes to display

Delete	Mapping To	Ontology	Source
	http://www.orpha.net/ORDO/Orphanet_98696	EFO	SAME_URI
	http://purl.obolibrary.org/obo/MONDO_0020266	MONDO	LOOM