OBO ID: DOID:0081023 |
Term Name: | retinal cone dystrophy 4 | Search Ontology: | |
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Definition: | A cone dystrophy that has_material_basis_in homozygous mutation in the CACNA2D4 gene on chromosome 12p13. https://pubmed.ncbi.nlm.nih.gov/26560832/ | ||
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Ontology: | Human Disease ( DOID:0081023 ) |
OTHER retinal cone dystrophy 4 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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