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Disease Ontology Browser
dominant pericentral pigmentary retinopathy (DOID:0110420)
Alliance: disease page
Alt IDs: OMIM:180210, ICD10CM:H35.5
Definition: A retinitis pigmentosa that is characterized pigmentary retinal degeneration with onset in the teens leading to blindness in the sixth ans seventh decades of life.

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
MGI 6.12
The Jackson Laboratory