Disease core ontology applied to Rare Diseases

Last uploaded: February 7, 2014

Preferred Name	Familial apolipoprotein C-II deficiency
Synonyms	ApoC-II deficiency
ID	http://www.limics.org/hrdo/rdfns#pat_id_21337
altLabel	ApoC-II deficiency
id_Medline	neant
id_MIM	207750
id_OMS	E78.3
id_Orpha	309020
patType	clinical subtype
prefixIRI	hrdo:pat_id_21337
prefLabel	Familial apolipoprotein C-II deficiency
subClassOf	http://www.limics.org/hrdo/rdfns#typ_id_2

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_309020	ORDO	LOOM
http://purl.bioontology.org/ontology/RCD/X40Vi	RCD	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/33513003	SNOMEDCT	LOOM
http://purl.obolibrary.org/obo/MONDO_0008810	CCONT	LOOM
http://purl.obolibrary.org/obo/MONDO_0008810	MONDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0008810	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0008810	DOVES	LOOM
http://purl.obolibrary.org/obo/DOID_0111418	DOID	LOOM
http://purl.obolibrary.org/obo/DOID_0111418	HHEAR	LOOM
http://purl.obolibrary.org/obo/DOID_0111418	DDSS	LOOM
http://purl.obolibrary.org/obo/DOID_0111418	NIFSTD	LOOM
http://purl.obolibrary.org/obo/DOID_0111418	FNS-H	LOOM
http://purl.bioontology.org/ontology/SNMI/D6-60420	SNMI	LOOM
http://www.owl-ontologies.com/unnamed.owl#RID17610	DERMLEX	LOOM