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Summary Literature (0)
DOID:0110356 - retinitis pigmentosa 18

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PRPF3 gene on chromosome 1q21.

Synonyms: RP18

Xenbase Genes : prpf3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011075 - retinitis pigmentosa 18


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), retinitis pigmentosa (is_a)