Term Name: Leber congenital amaurosis 12
Synonyms: LCA12
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the RD3 gene on chromosome 1q32.
Ontology: Human Disease [DOID:0110080]   ( DOID:0110080 )

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