OBO ID: DOID:0111005 |
Term Name: | cone-rod dystrophy 2 | Search Ontology: | |
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Definition: | A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/9390563 | ||
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Ontology: | Human Disease ( DOID:0111005 ) |
OTHER cone-rod dystrophy 2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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