retinitis pigmentosa 33

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Summary

Literature (0)

DOID:0110366 - retinitis pigmentosa 33

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the SNRNP200 gene on chromosome 2q11.

Synonyms: RP33

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

: snrnp200

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012477 - retinitis pigmentosa 33

MONDO:0012477 - retinitis pigmentosa 33

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)