Term Name: Leber congenital amaurosis 2
Synonyms: amaurosis congenita of Leber II, LCA2
Definition: A Leber congenital amaurosis that is characterized by night blindness, some transient improvement in vision, and eventual progressive visual loss and has_material_basis_in mutation in the RPE65 gene on chromosome 1.
Ontology: Human Disease [DOID:0110016]   ( DOID:0110016 )

Relationships
is a type of: autosomal recessive disease Leber congenital amaurosis