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Summary Literature (0)
DOID:0110368 - retinitis pigmentosa 26

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the CERKL gene on chromosome 2q31.

Synonyms: RP26

Xenbase Genes : cerkl

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012024 - retinitis pigmentosa 26

MIM:
MIM:608380 - RETINITIS PIGMENTOSA 26; RP26

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)