retinitis pigmentosa 41

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:0110376 - retinitis pigmentosa 41

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PROM1 gene on chromosome 4p15.

Synonyms: RP41

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

: prom1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012796 - retinitis pigmentosa 41

MONDO:0012796 - retinitis pigmentosa 41

MIM:

MIM:612095 - RETINITIS PIGMENTOSA 41; RP41

MIM:612095 - RETINITIS PIGMENTOSA 41; RP41

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)