retinitis pigmentosa 39

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Summary

Literature (0)

DOID:0110360 - retinitis pigmentosa 39

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the USH2A gene on chromosome 1q41.

Synonyms: RP39

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

: ush2a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013436 - retinitis pigmentosa 39

MONDO:0013436 - retinitis pigmentosa 39

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

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

Parent(s): retinitis pigmentosa (is_a)