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 -