retinitis pigmentosa 10

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Summary

Literature (0)

DOID:0110388 - retinitis pigmentosa 10

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the IMPDH1 gene on chromosome 7q32.

Synonyms: RP10

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

: impdh1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008379 - retinitis pigmentosa 10

MONDO:0008379 - retinitis pigmentosa 10

MIM:

MIM:180105 - RETINITIS PIGMENTOSA 10; RP10

MIM:180105 - RETINITIS PIGMENTOSA 10; RP10

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)