|OBO ID: DOID:14791|
|Term Name:||Leber congenital amaurosis||Search Ontology:|
|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|
|Ontology:||Human Disease (DOID:14791)|
|is a type of:||
OTHER Leber congenital amaurosis PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
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