Disease #03456 (LCA8 (Leber congenital amaurosis, type 8 (LCA-8)), OMIM:613835)
Official abbreviation |
LCA8 |
Name |
Leber congenital amaurosis, type 8 (LCA-8) |
OMIM ID |
613835 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
CRB1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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