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Summary Literature (0)
DOID:0110383 - retinitis pigmentosa 7

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21.

Synonyms: RP7

Xenbase Genes : rom1, prph2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011974 - epiphysis of proximal phalanx of pes

MIM:
MIM:608133 - RETINITIS PIGMENTOSA 7; RP7

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

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