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autosomal recessive pericentral pigmentary retinopathy

Disease Summary
Associated Targets ()

Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0009987:  autosomal recessive pericentral pigmentary retinopathy
MESH:C564838: 
UMLS:C1849398: