retinitis pigmentosa 41

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Echinobase

Summary

Literature (0)

DOID:0110376 - retinitis pigmentosa 41

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PROM1 gene on chromosome 4p15.

Synonyms: RP41

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

: prom1

MIM:

MIM:612095 - retinitis pigmentosa 41; rp41

MIM:612095 - retinitis pigmentosa 41; rp41

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)