OBO ID: DOID:0110422 |
Term Name: | autosomal recessive pericentral pigmentary retinopathy | Search Ontology: | |
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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. https://www.ncbi.nlm.nih.gov/pubmed/3189470 | ||
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Ontology: | Human Disease ( DOID:0110422 ) |
OTHER autosomal recessive pericentral pigmentary retinopathy PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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