Disease #02488 (LCA3;RP94 (Leber congenital amaurosis, type 3), OMIM:604232)
| Official abbreviation |
LCA3;RP94 |
| Name |
Leber congenital amaurosis, type 3 |
| OMIM ID |
604232 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
SPATA7 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2026-06-27 17:26:41 +02:00 (CEST) |
Individuals
|