OBO ID: DOID:0111017 |
Term Name: | cone-rod dystrophy 10 | Search Ontology: | |
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Definition: | A cone-rod dystrophy that has_material_basis_in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22. https://www.ncbi.nlm.nih.gov/pubmed/16199541 | ||
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Ontology: | Human Disease ( DOID:0111017 ) |
OTHER cone-rod dystrophy 10 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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