OBO ID: DOID:14791
Term Name: Leber congenital amaurosis Search Ontology:
Synonyms:
  • LCA
  • Leber's amaurosis
  • Leber's congenital amaurosis
  • Leber's disease
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
References:
Ontology: Human Disease   (DOID:14791)
OTHER Leber congenital amaurosis PAGES
GENES INVOLVED No data available
PHENOTYPE No data available

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