retinitis pigmentosa 2

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Summary

Literature (0)

DOID:0110415 - retinitis pigmentosa 2

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the RP2 gene on chromosome Xp11.3.

Synonyms: RP2

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

: rp2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010723 - retinitis pigmentosa 2

MONDO:0010723 - retinitis pigmentosa 2

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), X-linked monogenic disease (is_a)