Search Ontology:
Human Disease

Leber congenital amaurosis

Term ID
DOID:14791
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 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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