retinitis pigmentosa 70

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:0110392 - retinitis pigmentosa 70

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PRPF4 gene on chromosome 9q32.

Synonyms: RP70

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

: prpf4

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014400 - hepatic sinusoidal space

MONDO:0014400 - hepatic sinusoidal space

MIM:

MIM:615922 - RETINITIS PIGMENTOSA 70; RP70

MIM:615922 - RETINITIS PIGMENTOSA 70; RP70

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

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

Parent(s): autosomal dominant disease (is_a), retinitis pigmentosa (is_a)