retinitis pigmentosa 3

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:0110414 - retinitis pigmentosa 3

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the RPGR gene on chromosome Xp11.

Synonyms: RP3

Xenbase 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

: rpgr

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010227 - future cardiac atrium

MONDO:0010227 - future cardiac atrium

MIM:

MIM:300029 - RETINITIS PIGMENTOSA 3; RP3

MIM:300029 - RETINITIS PIGMENTOSA 3; RP3

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

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

Parent(s): retinitis pigmentosa (is_a)