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Disease Ontology Browser
retinitis pigmentosa 38 (DOID:0110367)
Alliance: disease page
Synonyms: RP38
Alt IDs: OMIM:613862, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the MERTK gene on chromosome 2q13.

Contributing Projects:
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