Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110399 - retinitis pigmentosa 37

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the NR2E3 gene on chromosome 15q23.

Synonyms: RP37

Xenbase Genes : nr2e3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012625 - retinitis pigmentosa 37

MIM:
MIM:611131 - RETINITIS PIGMENTOSA 37; RP37

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autosomal dominant disease (is_a), autosomal recessive disease (is_a), retinitis pigmentosa (is_a)