Cell Culture Ontology

Last uploaded: July 23, 2014

Preferred Name	autosomal recessive retinitis pigmentosa
Synonyms
Definitions	Autosomal recessive retinitis pigmentosa (RP) is an autosomally recessive inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades.
ID	http://www.ebi.ac.uk/efo/EFO_0020026
creator	zmp
database_cross_reference	SNOMEDCT:232053004 Medgen:C0339526
date	2021-10-28T07:43:55Z
definition	Autosomal recessive retinitis pigmentosa (RP) is an autosomally recessive inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades.
label	autosomal recessive retinitis pigmentosa
preferred label	autosomal recessive retinitis pigmentosa
prefixIRI	efo:EFO_0020026
prefLabel	autosomal recessive retinitis pigmentosa
subClassOf	http://www.orpha.net/ORDO/Orphanet_98657

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Mapping To	Ontology	Source
http://www.ebi.ac.uk/efo/EFO_0020026	EFO	SAME_URI
http://www.ebi.ac.uk/efo/EFO_0020026	EFO	SAME_URI
http://purl.bioontology.org/ontology/SNOMEDCT/232053004	SNOMEDCT	LOOM
http://www.ebi.ac.uk/efo/EFO_0020026	EFO	LOOM
http://www.ebi.ac.uk/efo/EFO_0020026	EFO	LOOM
http://purl.bioontology.org/ontology/RCD/X00dt	RCD	LOOM
http://nanbyodata.jp/ontology/NANDO_1200434	NANDO	LOOM