OBO ID: DOID:0112144 |
Term Name: | retinitis pigmentosa 87 | Search Ontology: | |
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Definition: | A retinitis pigmentosa characterized by slowly progressive visual disturbance and extensive choroid/retinal atrophy that has_material_basis_in heterozygous mutation in the RPE65 gene on chromosome 1p31.3. (2) | ||
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Ontology: | Human Disease ( DOID:0112144 ) |
OTHER retinitis pigmentosa 87 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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