| GTO ID(s) | GTC0315 | GTC1310 | GTC0478 | GTC2090 | GTC2668 | GTC0371 | GTC0590 | GTC0683 | GTC0585 | GTC3577 | GTC0037 | GTC3625 | GTC0132 |
| Disease Name | Leber Congenital Amaurosis |
| Synonyms | leber congenital amaurosis, congenital amaurosis of retinal origin |
| Definition | DO:A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness. |
| Xref | DO:14791 | MONDO:0018998 | MSH:D057130 | NCI:C129075 | ORDO:65 |
| Disease Group | Genetic Disease |