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Autosomal recessive pericentral pigmentary retinopathy

MONDO:0009987

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.

Also known as: retinitis pigmentosa, pericentral, retinopathy, pericentral pigmentary, autosomal recessive

25 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive pericentral pigmentary retinopathy itself.

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