red color blindness

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Echinobase

Summary

Literature (0)

DOID:13910 - red color blindness

Disease Ontology Definition:n_a

Synonyms: Protan defect, Protanopia

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: opn1lw

MIM:

MIM:303900 - colorblindness, partial, protan series; cbp

MIM:303900 - colorblindness, partial, protan series; cbp

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): color blindness (is_a)