retinitis pigmentosa 30

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Summary

Literature (0)

DOID:0110406 - retinitis pigmentosa 30

Disease Ontology Definition:A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25.

Synonyms: RP30

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

: fscn2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011935 - retinitis pigmentosa 30

MONDO:0011935 - retinitis pigmentosa 30

MIM:

MIM:607921 - RETINITIS PIGMENTOSA 30; RP30

MIM:607921 - RETINITIS PIGMENTOSA 30; RP30

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): retinitis pigmentosa (is_a)