retinitis pigmentosa 27

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Summary

Literature (0)

DOID:0110397 - retinitis pigmentosa 27

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the NRL gene on chromosome 14q11.

Synonyms: RP27

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

: nrl

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013402 - retinitis pigmentosa 27

MONDO:0013402 - retinitis pigmentosa 27

MIM:

MIM:613750 - RETINITIS PIGMENTOSA 27; RP27

MIM:613750 - RETINITIS PIGMENTOSA 27; RP27

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)