retinitis pigmentosa 11

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Summary

Literature (0)

DOID:0110408 - retinitis pigmentosa 11

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the PRPF31 gene on chromosome 19q13.

Synonyms: RP11

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

: prpf31

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010828 - retinitis pigmentosa 11

MONDO:0010828 - retinitis pigmentosa 11

MIM:

MIM:600138 - RETINITIS PIGMENTOSA 11; RP11

MIM:600138 - RETINITIS PIGMENTOSA 11; RP11

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)