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Disease Ontology Browser
autosomal recessive pericentral pigmentary retinopathy (DOID:0110422)
Alt IDs: OMIM:268060, ICD10CM:H35.5, ORDO:791
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.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory