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Summary Literature (0)
DOID:0112144 - retinitis pigmentosa 87

Disease Ontology Definition:A retinitis pigmentosa characterized by slowly progressive visual disturbance and extensive choroid/retinal atrophy that has_material_basis_in heterozygous mutation in the RPE65 gene on chromosome 1p31.3.

Synonyms: retinitis pigmentosa 87 with choroidal involvement, RP87

Xenbase Genes :


MIM:
MIM:618697 - RETINITIS PIGMENTOSA 87 WITH CHOROIDAL INVOLVEMENT; RP87

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)