Disease #00702 (LCA-10 (Leber congenital amaurosis, type 10 (LCA-10)), OMIM:611755)
Official abbreviation |
LCA-10 |
Name |
Leber congenital amaurosis, type 10 (LCA-10) |
OMIM ID |
611755 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
CEP290 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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