Disease core ontology applied to Rare Diseases

Last uploaded: February 7, 2014

Preferred Name	Autosomal recessive cerebellar ataxia due to a DNA repair defect
Synonyms
ID	http://www.limics.org/hrdo/rdfns#pat_id_13115
id_Medline	neant
id_OMS	G11.3
id_Orpha	98097
patType	group of phenomes
prefixIRI	hrdo:pat_id_13115
prefLabel	Autosomal recessive cerebellar ataxia due to a DNA repair defect
subClassOf	http://www.limics.org/hrdo/rdfns#pat_id_3711

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_98097	CCONT	LOOM
http://www.orpha.net/ORDO/Orphanet_98097	EFO	LOOM
http://www.orpha.net/ORDO/Orphanet_98097	ORDO	LOOM