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Summary Literature (0)
DOID:0110376 - retinitis pigmentosa 41

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PROM1 gene on chromosome 4p15.

Synonyms: RP41,

Xenbase Genes : prom1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012796 - retinitis pigmentosa 41


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

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