Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024

Preferred Name	Autosomal recessive congenital cerebellar ataxia
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_98095
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=98095
hasDbXref	UMLS:C5681519
label	Autosomal recessive congenital cerebellar ataxia
notation	ORPHA:98095 Category
prefixIRI	ORDO:Orphanet_98095
prefLabel	Autosomal recessive congenital cerebellar ataxia
subClassOf	http://www.orpha.net/ORDO/Orphanet_1172 http://www.orpha.net/ORDO/Orphanet_557492

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_98095	CCONT	SAME_URI
http://www.orpha.net/ORDO/Orphanet_98095	EFO	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0020043	MONDO	LOOM
http://www.limics.org/hrdo/rdfns#pat_id_13113	HRDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0020043	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0020043	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0020043	DOVES	LOOM
http://purl.obolibrary.org/obo/MONDO_0020043	KTAO	LOOM