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Disease Ontology Browser
retinitis pigmentosa 30 (DOID:0110406)
Alliance: disease page
Synonyms: RP30
Alt IDs: OMIM:607921, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.13
The Jackson Laboratory