Cell Culture Ontology

Last uploaded: July 23, 2014

Preferred Name	familial chylomicronemia syndrome
Synonyms
ID	http://purl.obolibrary.org/obo/MONDO_0018637
database_cross_reference	DOID:0111417 Orphanet:444490 UMLS:C5442313 MEDGEN:1778100 GARD:6414
id	MONDO:0018637
in_subset	http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#otar http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare http://purl.obolibrary.org/obo/mondo/mondo-base#orphanet_rare http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_disorder
label	familial chylomicronemia syndrome
notation	MONDO:0018637
preferred label	familial chylomicronemia syndrome
prefLabel	familial chylomicronemia syndrome
skos_exactMatch	http://purl.obolibrary.org/obo/Orphanet_444490 http://linkedlifedata.com/resource/umls/id/C5442313 http://purl.obolibrary.org/obo/DOID_0111417 http://identifiers.org/medgen/1778100
subClassOf	http://purl.obolibrary.org/obo/MONDO_0002254

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0018637	MONDO	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018637	EFO	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018637	DOVES	SAME_URI
http://purl.bioontology.org/ontology/SNOMEDCT/1197489003	SNOMEDCT	LOOM
http://purl.obolibrary.org/obo/MONDO_0018637	MONDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0018637	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0018637	DOVES	LOOM
http://purl.bioontology.org/ontology/MEDDRA/10085051	MEDDRA	LOOM
http://purl.obolibrary.org/obo/DOID_0111417	DOID	LOOM
http://purl.obolibrary.org/obo/DOID_0111417	BAO	LOOM
http://purl.obolibrary.org/obo/DOID_0111417	HHEAR	LOOM
http://purl.obolibrary.org/obo/DOID_0111417	DDSS	LOOM
http://purl.obolibrary.org/obo/DOID_0111417	NIFSTD	LOOM
http://purl.obolibrary.org/obo/DOID_0111417	FNS-H	LOOM
http://www.orpha.net/ORDO/Orphanet_444490	ORDO	LOOM