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Summary Literature (0)
DOID:0110363 - retinitis pigmentosa 71

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the IFT172 gene on chromosome 2p23.

Synonyms: RP71

Xenbase Genes : ift172

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014618 - retinitis pigmentosa 71


Other Model Organisms: Alliance, 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)