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Summary Literature (0)
DOID:0110372 - retinitis pigmentosa 4


Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the RHO gene on chromosome 3q22.

Synonyms: RP4

Referenced OMIM:
OMIM:613731 - RETINITIS PIGMENTOSA 4; RP4

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

Xenbase Genes : rho, rho.2

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


Xenbase: The Xenopus Model Organism Knowledgebase.
Version: 4.15.0
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