Disease #03450 (LCA6 (Leber congenital amaurosis, type 6 (LCA-6)), OMIM:613826)
Official abbreviation |
LCA6 |
Name |
Leber congenital amaurosis, type 6 (LCA-6) |
OMIM ID |
613826 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
10 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
RPGRIP1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|