OBO ID: DOID:14791 |
Term Name: | Leber congenital amaurosis | Search Ontology: | |
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Definition: | A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness. http://en.wikipedia.org/wiki/Leber%27s_congenital_amaurosis | ||
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Ontology: | Human Disease ( DOID:14791 ) |
OTHER Leber congenital amaurosis PAGES
GENES INVOLVED
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ZEBRAFISH MODELS
PHENOTYPE
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CITATIONS (9)
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