Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024

Preferred Name	Ocular albinism
Synonyms
ID	http://www.orpha.net/ORDO/Orphanet_284804
expertlink	https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=284804
hasDbXref	MedDRA:10065276 ICD-11:9E1Y UMLS:C0078917 MeSH:D016117
label	Ocular albinism
notation	ORPHA:284804 Clinical group
prefixIRI	ORDO:Orphanet_284804
prefLabel	Ocular albinism
subClassOf	http://www.orpha.net/ORDO/Orphanet_352728 http://www.orpha.net/ORDO/Orphanet_557492 http://www.orpha.net/ORDO/Orphanet_98706

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://www.orpha.net/ORDO/Orphanet_284804	EFO	SAME_URI
http://purl.bioontology.org/ontology/MEDDRA/10065276	MEDDRA	LOOM
http://purl.obolibrary.org/obo/MP_0006159	MP	LOOM
http://purl.obolibrary.org/obo/MP_0006159	UPHENO	LOOM
http://purl.obolibrary.org/obo/MP_0006159	CHIRO	LOOM
http://www.limics.org/hrdo/rdfns#pat_id_20623	HRDO	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/26399002	SNOMEDCT	LOOM
http://purl.obolibrary.org/obo/DOID_0050633	DTO	LOOM
http://purl.obolibrary.org/obo/DOID_0050633	BAO	LOOM
http://purl.obolibrary.org/obo/DOID_0050633	MIDO	LOOM
http://purl.obolibrary.org/obo/DOID_0050633	FNS-H	LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0078917	OCHV	LOOM
http://purl.bioontology.org/ontology/RCTV2/P3y0.00	RCTV2	LOOM
http://purl.bioontology.org/ontology/RCD/P3y0.	RCD	LOOM
http://purl.obolibrary.org/obo/MONDO_0017304	EFO	LOOM
http://purl.obolibrary.org/obo/MONDO_0017304	MONDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0017304	DOVES	LOOM
http://purl.obolibrary.org/obo/HP_0001107	HP	LOOM
http://purl.obolibrary.org/obo/HP_0001107	UPHENO	LOOM
http://purl.obolibrary.org/obo/HP_0001107	OBA	LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:0346	IFAR	LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU037236	OMIM	LOOM
http://purl.bioontology.org/ontology/ICD10CM/E70.31	ICD10CM	LOOM
http://www.phoc.org.cn/pmo/class/PMO_00006845	PMAPP-PMO	LOOM