retinitis pigmentosa 59

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Summary

Literature (0)

DOID:0110352 - retinitis pigmentosa 59

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the DHDDS gene on chromosome 1p36.11.

Synonyms: RP59

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: dhdds

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013468 - retinitis pigmentosa 59

MONDO:0013468 - retinitis pigmentosa 59

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)