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Disease Ontology Browser
autosomal recessive pericentral pigmentary retinopathy (DOID:0110422)
Alliance: disease page
Alt IDs: OMIM:268060, ICD10CM:H35.5
Definition: A retinitis pigmentosa that is characterized autosomal recessive inheritance of pigmentary retinal degeneration with onset in the infancy but slower rates of progression than other forms of retinopathy.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.17
The Jackson Laboratory