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:0110371 - retinitis pigmentosa 56

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the IMPG2 gene on chromosome 3q12.3.

Synonyms: RP56

Xenbase Genes : impg2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013314 - retinitis pigmentosa 56

MIM:
MIM:613581 - RETINITIS PIGMENTOSA 56; RP56

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

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