retinitis pigmentosa 13

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Summary

Literature (0)

DOID:0110403 - retinitis pigmentosa 13

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutations in the PRPF8 gene on chromosome 17p13.3.

Synonyms: RP13

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

: prpf8

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010806 - retinitis pigmentosa 13

MONDO:0010806 - retinitis pigmentosa 13

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)