retinitis pigmentosa 60

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Summary

Literature (0)

DOID:0110411 - retinitis pigmentosa 60

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PRPF6 gene on chromosome 20q13.33.

Synonyms: RP60

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

: prpf6

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013516 - retinitis pigmentosa 60

MONDO:0013516 - retinitis pigmentosa 60

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)