OBO ID: DOID:0110367 |
Term Name: | retinitis pigmentosa 38 | Search Ontology: | |
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Definition: | A retinitis pigmentosa that has_material_basis_in mutation in the MERTK gene on chromosome 2q13. https://www.ncbi.nlm.nih.gov/pubmed/11062461 | ||
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Ontology: | Human Disease ( DOID:0110367 ) |
OTHER retinitis pigmentosa 38 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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