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Disease Ontology Browser
retinitis pigmentosa-deafness syndrome (DOID:0110829)
Alliance: disease page
Alt IDs: OMIM:500004, ICD10CM:H35.5, ORDO:231183, UMLS_CUI:C1568248
Definition: An Usher syndrome characterized by retinitis pigmentosa and onset of sensorineural hearing impairment in the teens that has_material_basis_in mutation in the MTTS2 gene in the mitochondrial genome.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory