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Preferred Name

opsin 1, medium wave sensitive
ID

http://www.orpha.net/ORDO/Orphanet_124012
alternative_term

COD5

OPN1MW1

cone dystrophy 5 (X-linked)
hasDbXref

Genatlas:OPN1MW

IUPHAR:2962

Ensembl:ENSG00000268221

HGNC:4206

Reactome:P04001

OMIM:300821

SwissProt:P04001
label

opsin 1, medium wave sensitive
prefixIRI

ORDO:Orphanet_124012
prefLabel

opsin 1, medium wave sensitive
symbol

OPN1MW
subClassOf

http://www.orpha.net/ORDO/Orphanet_410298
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/300821 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM