OBO ID: DOID:0112142 |
Term Name: | retinitis pigmentosa 85 | Search Ontology: | |
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Definition: | A retinitis pigmentosa that has_material_basis_in homozygous or compound heterozygous mutation in AHR on chromosome 7p21.1. https://pubmed.ncbi.nlm.nih.gov/29726989/ | ||
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Ontology: | Human Disease ( DOID:0112142 ) |
OTHER retinitis pigmentosa 85 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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