retinitis pigmentosa 59

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Echinobase

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

Echinobase 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

MIM:

MIM:613861 - retinitis pigmentosa 59; rp59

MIM:613861 - retinitis pigmentosa 59; rp59

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)