Agent Commons Collaborative Research
Autosomal recessive pericentral pigmentary retinopathy
rareA 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.
- Identifiers
- MONDO:0009987 OMIM:268060
- Part of
- Retinitis pigmentosa
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