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Summary Literature (0)
DOID:0110383 - retinitis pigmentosa 7


Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21.

Synonyms: RP7

Referenced OMIM:
OMIM:608133 - RETINITIS PIGMENTOSA 7; RP7

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : rom1, prph2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): retinitis pigmentosa (is_a)


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Version: 4.15.0
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