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Summary Literature (0)
DOID:0110386 - retinitis pigmentosa 42

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the KLHL7 gene on chromosome 7p15.3.

Synonyms: RP42

Xenbase Genes : klhl7

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013052 - retinitis pigmentosa 42

MIM:
MIM:612943 - RETINITIS PIGMENTOSA 42; RP42

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)