OBO ID: DOID:0110403 |
Term Name: | retinitis pigmentosa 13 | Search Ontology: | |
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Definition: | A retinitis pigmentosa that has_material_basis_in mutations in the PRPF8 gene on chromosome 17p13.3. https://www.ncbi.nlm.nih.gov/pubmed/11468273 | ||
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Ontology: | Human Disease ( DOID:0110403 ) |
OTHER retinitis pigmentosa 13 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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