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Disease Ontology Browser
retinitis pigmentosa 42 (DOID:0110386)
Synonyms: RP42
Alt IDs: OMIM:612943, ICD10CM:H35.5, ORDO:791
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the KLHL7 gene on chromosome 7p15.3.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/18/2017
MGI 6.08
The Jackson Laboratory