DISEASES

Disease-gene associations mined from literature

Human genes for Leber congenital amaurosis

Leber congenital amaurosis [DOID:14791]

A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness.

Synonyms:  Leber congenital amaurosis,  DOID:14791,  LCA,  Leber congenital amaurosis type 13,  Leber congenital amaurosis type 14 ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10 #11 #12 #13 #14 #15 #16 #17