retinitis pigmentosa 20

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Summary

Literature (0)

DOID:0110353 - retinitis pigmentosa 20

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the RPE65 gene on chromosome 1p31.

Synonyms: RP20

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

: rpe65

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013425 - retinitis pigmentosa 20

MONDO:0013425 - retinitis pigmentosa 20

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)